Genetic markers for engraftment of human cardiac ventricular progenitor cells

ABSTRACT

The present invention provides genetic markers for identifying engraftable human cardiac ventricular progenitor cells. The engraftment markers of the invention include angiogenic markers and extracellular matrix markers. Human ventricular progenitor cells expressing these markers are capable of forming ventricular tissue in vivo that is vascularized and supported by an extracellular matrix. Methods of engrafting human cardiac ventricular progenitor cells by transplanting into a subject progenitor cells that express the engraftment markers are also provided.

CROSS REFERENCE TO RELATED APPLICATION

This application is a continuation of U.S. application Ser. No. 15/433,713, filed on Feb. 15, 2017, which claims priority to, and the benefit of, U.S. Application No. 62/297,217, filed on Feb. 19, 2016. The contents of these applications are hereby incorporated herein by reference in its entirety.

BACKGROUND OF THE INVENTION

Heart failure, predominantly caused by myocardial infarction, is the leading cause of death in both adults and children worldwide and is increasing exponentially worldwide (Bui, A. L. et al. (2011) Nat. Rev. Cardiol. 8:30-41). The disease is primarily driven by the loss of ventricular muscle that occurs during myocardial injury (Lin, Z. and Pu, W. T. (2014) Sci. Transl. Med. 6:239rv1) and is compounded by the negligible ability of the adult heart to mount a regenerative response (Bergmann, O. et al. (2009) Science 324:98-102; Senyo, S. E. et al. (2013) Nature 493:433-436). Although heart transplantation can be curative, the markedly limited availability of human heart organ donors has led to a widespread unmet clinical need for a renewable source of pure, mature and functional human ventricular muscle tissue (Segers, V. F. M. and Lee, R. J. (2008) Nature 451:937-942; Spater, D. et al. (2014) Development 141:4418-4431).

Human pluripotent stem cells (hPSCs) offer the potential to generate large numbers of functional cardiomyocytes for potential clinical restoration of function in damaged or diseased hearts. Transplantation of stem cells into the heart to improve cardiac function and/or to enrich and regenerate damaged myocardium has been proposed (see e.g., U.S. Patent Publication 20040180043). Combination therapy, in which adult stem cells are administered in combination with treatment with growth factor proteins has also been proposed (see e.g., U.S. Patent Publication 20050214260).

A significant advancement in the approach of cell transplantation to improve cardiac function and regenerate heart tissue was the identification and isolation of a family of multipotent cardiac progenitor cells that are capable of giving rise to cardiac myocytes, cardiac smooth muscle and cardiac endothelial cells (Cal, C. L. et al. (2003) Dev. Cell. 5:877-889; Moretti, A. et al. (2006) Cell 127:1151-1165; Bu, L. et al. (2009) Nature 460:113-117; U.S. Patent Publication 20060246446). These cardiac progenitor cells are characterized by the expression of the LIM homeodomain transcription factor Islet 1 (Isl1) and thus are referred to as Isl1+ cardiac progenitor cells. (Ibid). In contrast, Isl1 is not expressed in differentiated cardiac cells. Additional markers of the Isl1+ cardiac progenitor cells that arise later in differentiation than Isl1 have been described and include Nkx2.5 and flk1 (see e.g., U.S. Patent Publication 20100166714).

The renewal and differentiation of Isl1+ cardiac progenitor cells has been shown to be regulated by a Wnt/beta-catenin signaling pathway (see e.g., Qyang, Y. et al. (2007) Cell Stem Cell. 1:165-179; Kwon, C. et al. (2007) Proc. Natl. Acad. Sci. USA 104:10894-10899). This has led to the development of methods to induce a pluripotent stem cell to enter the Isl1+ lineage and for expansion of the Isl1+ population through modulation of Wnt signaling (see e.g., Lian, X. et al. (2012) Proc. Natl. Acad. Sci. USA 109:E1848-57; Lian, X. et al. (2013) Nat. Protoc. 8:162-175; U.S. Patent Publication 20110033430; U.S. Patent Publication 20130189785).

While human pluripotent stem cells hold great promise, a significant challenge has been the ability to move from simply differentiation of diverse cardiac cells to forming a larger scale pure 3D ventricular muscle tissue in vivo, which ultimately requires vascularization, assembly and alignment of an extracellular matrix, and maturation. Toward that end, a diverse population of cardiac cells (atrial, ventricular, pacemaker) has been coupled with artificial and decellurized matrices (Masumoto, H. et al. (2014) Sci. Rep. 4:5716; Ott, H. C. et al. (2008) Nat. Med. 14:213-221; Schaaf, S. et al. (2011) PLoS One 6:e26397), vascular cells and conduits (Tulloch, N. L. et al. (2011) Circ. Res. 109:47-59) and cocktails of microRNAs (Gama-Garvalho, M. et al. (2014) Cells 3:996-1026) have been studied, but the goal remains elusive.

Accordingly, there is still a need in the art for genetics markers of cardiac progenitor cells that would allow for identification of those cells that can successfully form a tissue graft in vivo, in particular genetic markers for identification of progenitor cells that can differentiate into ventricular muscle cells, as well as achieve vascularization and extracellular matrix formation in vivo.

SUMMARY OF THE INVENTION

This invention provides genetic markers, referred to as engraftment markers, that identify human ventricular progenitor cells (HVPs) which have the capacity to engraft in vivo. Transplantation of the HVPs in vivo generates a graft of mature ventricular muscle tissue that is vascularized and has an extracellular matrix. HVPs have previously been shown to express cell surface markers such as JAG1, FZD4, LIFR, FGFR3 and/or TNFSF9, as well as the intracellular marker Islet 1 (see U.S. Ser. No. 14/832,324, filed Aug. 21, 2015, and U.S. Ser. No. 14/984,783, filed Dec. 30, 2015, the entire contents of each of which are expressly incorporated herein by reference). The engraftment markers of the invention now allow for the identification of cells within that population which have the capacity for engraftment. In one embodiment, the engraftment marker is an angiogenic marker. In another embodiment, the engraftment marker is an extracellular matrix marker. The invention provides both “positive” markers, whose expression strongly correlates with the expression of other HVP markers to thereby allow for identification of engraftable HVPs, as well as “negative” markers, whose lack of expression strongly correlates with the expression of other HVP markers to thereby also allow for identification of engraftable HVPs.

Accordingly, in one aspect, the invention provides a method of identifying engraftable human ventricular progenitor cells (HVPs), the method comprising:

-   -   detecting expression of at least one engraftment marker in the         HVPs to thereby identify engraftable HVPs, wherein:     -   the HVPs also express at least one surface marker selected from         the group consisting of: JAG1, FZD4, LIFR, FGFR3 and/or TNFSF9.

In another aspect, the invention provides a method of isolating engraftable human ventricular progenitor cells (HVPs), the method comprising:

-   -   culturing human cells containing cardiac progenitor cells under         conditions causing differentiation into human ventricular         progenitor cells (HVPs);     -   detecting expression on the HVPs of at least one surface marker         selected from the group consisting of JAG1, FZD4, LIFR, FGFR3         and/or TNFSF9;     -   detecting expression in the HVPs of at least one engraftment         marker; and     -   isolating HVPs that co-express the at least one surface marker         and the at least one engraftment marker to thereby isolate         engraftable HVPs.

In another aspect, the invention provides a method for engrafting human ventricular tissue in a subject, the method comprising:

-   -   transplanting engraftable human ventricular progenitor cells         (HVPs) into the subject such that human ventricular tissue is         engrafted in the subject,     -   wherein prior to transplantation, engraftable HVPs are         identified by detecting expression of at least one engraftment         marker in the HVPs; and     -   wherein the HVPs express at least one surface marker selected         from the group consisting of: JAG1, FZD4, LIFR, FGFR3 and/or         TNFSF9.

In another aspect, the invention provides a method for engrafting human ventricular tissue in a subject, the method comprising:

-   -   culturing human cells containing cardiac progenitor cells under         conditions causing differentiation into human ventricular         progenitor cells (HVPs);     -   detecting expression on the HVPs of at least one surface marker         selected from the group consisting of JAG1, FZD4, LIFR, FGFR3         and/or TNFSF9;     -   detecting expression in the HVPs of at least one engraftment         marker;     -   isolating HVPs that co-express the at least one surface marker         and the at least one engraftment marker to thereby isolate         engraftable HVPs; and     -   transplanting engraftable the HVPs into the subject such that         human ventricular tissue is engrafted in the subject.

In another aspect, the invention provides a method for engrafting human ventricular tissue in a subject, the method comprising:

-   -   culturing human cells containing cardiac progenitor cells under         conditions causing differentiation into human ventricular         progenitor cells (HVPs) expressing at least one surface marker         selected from the group consisting of JAG1, FZD4, LIFR, FGFR3         and/or TNFSF9;     -   isolating the HVPs expressing the at least one surface marker to         form an HVP population;     -   detecting expression of at least one engraftment marker in a         sample of the HVP population; and     -   transplanting the HVPs expressing the at least one surface         marker and the at least one engraftment marker into the subject         such that human ventricular tissue is engrafted in the subject.

In one embodiment, the at least one engraftment marker detected is at least one positive angiogenic marker. More than one positive angiogenic marker can be detected, for example, three or more, or ten or more, positive angiogenic markers can be detected.

In another embodiment, the at least one engraftment marker detected is at least one positive extracellular matrix marker. More than one positive extracellular matrix marker can be detected, for example, three or more, or ten or more, positive extracellular matrix markers can be detected.

In another embodiment, the at least one engraftment marker detected is at least one positive angiogenic marker and at least one positive extracellular matrix marker. More than one of each positive marker (angiogenic and extracellular matrix) can be detected, for example, three or more, or ten or more, of each of these positive markers can be detected.

In one embodiment, the at least one positive angiogenic marker is selected from the group consisting of: FGF10, PRKD1, CCBE1, PDGFRA, EPHB2, GATA2, NTRK1, PTGIS, BMPER, BMP4, C1GALT1, MEIS1, TBX1, PKNOX1, ID1, TCF21, HEY1, HOXB3, HGF, IL6, GHRL, IHH, SRPK2, GATA6, HAND1, AMOT, NRP2, PTEN, SEMA3E, APOLD1, SETD2, DAB2IP, KDR, PGF, EMP2, TAL1, ACVR1, HIPK2, CSPG4, TNFAIP3, NRP1, NFATC4, CDC42, ANGPTL4, BCAS3, HIPK1, NRXN3, FZD5 and HHEX. In another embodiment, the at least one positive angiogenic marker is selected from the group consisting of: FGF10, PRKD1, CCBE1, PDGFRA, EPHB2, GATA2, NTRK1, PTGIS, BMPER, BMP4, C1GALT1, MEIS1, TBX1, PKNOX1, ID1, TCF21 and HEY1. In another embodiment, the at least positive angiogenic marker is selected from the group consisting of: FGF10, PRKD1, CCBE1, PDGFRA, EPHB2, GATA2 and NTRK1.

In one embodiment, the at least one positive extracellular matrix marker is selected from the group consisting of: FGF10, SMOC1, CCBE1, COL6A6, ADAMTS12, COL19A1, LAMA1, BMP4, FBLN7, FBLN2, NDNF, HTRA1, HAPLN1, EMILIN1, SPOCK3, PODNL1, IHH, ACAN, NID2, COL4A6, LAMC1, FMOD, MUC4, EMID1, HMCN1, NID1, VCAN, CILP2, SOD3, ADAMTS3, ZP3, ANGPTL4, CRTAC1, LTBP4 and FREM1. In another embodiment, the at least one positive extracellular matrix marker is selected from the group consisting of: FGF10, SMOC1, CCBE1, COL6A6, ADAMTS12, COL19A1, LAMA1, BMP4, FBLN7, FBLN2, NDNF and HTRA1. In another embodiment, the at least one positive extracellular matrix marker is selected from the group consisting of: FGF10, SMOC1 and CCBE1.

In those embodiments in which both at least one positive angiogenic marker and at least one positive extracellular matrix marker are detected, the at least one positive angiogenic marker can be selected from the group consisting of: FGF10, PRKD1, CCBE1, PDGFRA, EPHB2, GATA2, NTRK1, PTGIS, BMPER, BMP4, C1GALT1, MEIS1, TBX1, PKNOX1, ID1, TCF21, HEY1, HOXB3, HGF, IL6, GHRL, IHH, SRPK2, GATA6, HAND1, AMOT, NRP2, PTEN, SEMA3E, APOLD1, SETD2, DAB2IP, KDR, PGF, EMP2, TAL1, ACVR1, HIPK2, CSPG4, TNFAIP3, NRP1, NFATC4, CDC42, ANGPTL4, BCAS3, HIPK1, NRXN3, FZD5 and HHEX; and

the at least one positive extracellular matrix marker can be selected from the group consisting of: FGF10, SMOC1, CCBE1, COL6A6, ADAMTS12, COL19A1, LAMA1, BMP4, FBLN7, FBLN2, NDNF, HTRA1, HAPLN1, EMILIN1, SPOCK3, PODNL1, IHH, ALAN, NID2, COL4A6, LAMC1, FMOD, MUC4, EMID1, HMCN1, NID1, VCAN, CILP2, SOD3, ADAMTS3, ZP3, ANGPTL4, CRTAC1, LTBP4 and FREM1.

In another embodiment, the at least one positive angiogenic marker is selected from the group consisting of: FGF10, PRKD1, CCBE1, PDGFRA, EPHB2, GATA2, NTRK1, PTGIS, BMPER, BMP4, C1GALT1, MEIS1, TBX1, PKNOX1, ID1, TCF21 and HEY1; and the at least one positive extracellular matrix marker is selected from the group consisting of: FGF10, SMOC1, CCBE1, COL6A6, ADAMTS12, COL19A1, LAMA1, BMP4, FBLN7, FBLN2, NDNF and HTRA1.

In another embodiment, the at least one positive angiogenic marker is selected from the group consisting of: FGF10, PRKD1, CCBE1, PDGFRA, EPHB2, GATA2 and NTRK1; and

the at least one positive extracellular matrix marker is selected from the group consisting of: FGF10, SMOC1 and CCBE1.

In one embodiment, the at least one engraftment marker detected is at least one negative angiogenic marker. More than one negative angiogenic marker can be detected, for example, three or more, or ten or more, negative angiogenic markers can be detected.

In another embodiment, the at least one engraftment marker detected is at least one negative extracellular matrix marker. More than one negative extracellular matrix marker can be detected, for example, three or more, or ten or more, negative extracellular matrix markers can be detected.

In another embodiment, the at least one engraftment marker detected is at least one negative angiogenic marker and at least one negative extracellular matrix marker. More than one of each negative marker (angiogenic and extracellular matrix) can be detected, for example, three or more, or ten or more, of each of these negative markers can be detected.

In one embodiment, the at least one negative angiogenic marker is selected from the group consisting of: ETS1, BAX, XBP1, TDGF1, C5AR1, EPHA1, HS6ST1, SHC1, SP100, JAM3, CASP8, FLT4, SFRP2, HPSE, BAK1, GPX1, VAV3, VAV2, EGF, ADAM15 and AGGF1. In another embodiment, the at least one negative angiogenic marker is selected from the group consisting of: VAV3, VAV2, EGF, ADAM15 and AGGF1.

In one embodiment, the at least one negative extracellular matrix marker is selected from the group consisting of: FKBP1A, CLU, TFP12, PLSCR1, FBLN5, VWA1, ADAMTS16, MMP25, SFRP2 and SOD1.

In those embodiments in which both at least one negative angiogenic marker and at least one negative extracellular matrix marker are detected, the at least one negative angiogenic marker can be selected from the group consisting of: ETS1, BAX, XBP1, TDGF1, C5AR1, EPHA1, HS6ST1, SHC1, SP100, JAM3, CASP8, FLT4, SFRP2, HPSE, BAK1, GPX1, VAV3, VAV2, EGF, ADAM15 and AGGF1; and the at least one negative extracellular matrix marker can be selected from the group consisting of: FKBP1A, CLU, TFP12, PLSCR1, FBLN5, VWA1, ADAMTS16, MMP25, SFRP2 and SOD1.

In one embodiment, detecting expression of at least one engraftment marker comprises detecting expression of mRNA encoding the at least one engraftment marker in the HVPs (detection of “positive” marker expression, such as a positive angiogenic marker(s) and/or a positive extracellular matrix marker(s)). In another embodiment, detecting expression of at least one engraftment marker comprises detecting lack of expression of mRNA encoding the at least one engraftment marker in the HVPs (detection of “negative” marker expression, such as a negative angiogenic marker(s) and/or a negative extracellular matrix marker(s)).

Other features and advantages of the invention will be apparent from the following detailed description and claims.

BRIEF DESCRIPTION OF THE DRAWING

The drawing is a schematic diagram of an exemplary culturing protocol for generating human Isl1+ cardiomyogenic progenitor cells from human pluripotent stem cells (hPSCs).

DETAILED DESCRIPTION OF THE INVENTION

The invention provides methods of identifying engraftable human ventricular progenitor cells (HVPs), as well as methods of transplanting engraftable HVPs. The methods of the invention are based, at least in part, on the discovery of the gene expression profile within those HVPs having the capacity, when transplanted in vivo, to form a graft of mature human ventricular tissue that is vascularized and has an extracellular matrix. Accordingly, detection of one or more engraftment markers in HVPs prior to transplantation allows for identification of those cells capable of engraftment in vivo, thereby greatly increasing the likelihood of success of the grafting process.

In order that the present invention may be more readily understood, certain terms are first defined. Additional definitions are set forth throughout the detailed description.

As used herein, the term “engraftable” refers to a property of cells (such as a human ventricular progenitor cells) relating to the ability to form a graft in vivo when transplanted into a host. Within a mixed population of cells (e.g., progenitor cells), not all cells within that mixed population will necessarily form a graft when transplanted into a host, since there are a number of biological processes that must occur for there to be successful engraftment. These biological processes include the formation of blood vessels into the graft (neovascularization) and the formation of an extracellular matrix to support the graft. Thus, the “engraftable” cells within a mixed population of cells refers to those cells having the capacity to form a graft in vivo when transplanted into a host.

As used herein, the term “engraftment marker” refers to a marker, such as a genetic or protein marker, detectable within cells that correlates with the engraftability of the cells, i.e., the ability of the cells to form a graft in vivo when transplanted into a host.

As used herein, an engraftment marker can be a “positive marker”, which refers to those markers whose expression positively correlates with other identifying markers of human ventricular progenitor cells (HVPs), such as the cell surface markers JAG1, FRZ4, LIFR and/or FGFR3, or the intracellular marker Islet 1. Alternatively, as used herein, an engraftment marker can be a “negative marker”, which refers to those markers whose expression negatively correlates with other identifying markers of human ventricular progenitor cells (HVPs), such as the cell surface markers JAG1, FRZ4, LIFR and/or FGFR3, or the intracellular marker Islet 1.

As used herein, the term “angiogenic marker” refers to a subcategory of engraftment marker in which the angiogenic marker is a gene or protein known to be involved in the process of angiogenesis.

As used herein, the term “extracellular matrix marker” refers to a subcategory of engraftment marker in which the extracellular matrix marker is a gene or protein known to be involved in the process of deposition of an extracellular matrix.

As used herein, the terms “Jagged 1”, “Jag 1” and “JAG 1” are used interchangeably to refer to a protein known in the art that has been described in, for example, Oda, T. et al. (1997) Genomics, 43:376-379; Oda, T. et al. (1997) Nat. Genet. 16:235-242; Li, L. et al. (1998) Immunity, 8:43-55; Bash, J. et al. (1999) EMBO J., 18:2803-2811; and Jones, E. A. et al. (2000) J. Med. Genet. 37:658-662. A non-limiting example of a Jagged 1 protein is the human protein having the amino acid sequence set forth in Genbank Accession Number P78504.3.

As used herein, the terms “Frizzled 4”, “Fzd 4” and “FZD 4” are used interchangeably to refer to a protein known in the art that has been described in, for example, Kinkoshi, H. et al. (1999) Biochem. Biophys. Res. Commun., 264:955-961; Tanaka, S. et al. (1998) Proc. Natl. Acad. Sci. USA 95:10164-10169; and Robitaille, J. et al. (2002) Nat. Genet., 32:326-330. A non-limiting example of a Frizzled 4 protein is the human protein having the amino acid sequence set forth in Genbank Accession Number Q9ULV1.

As used herein, the terms “Leukemia Inhibitor Factor Receptor”, “LIF Receptor” and “LIFR” are used interchangeably to refer to a protein known in the art that has been described in, for example, Gearing, D. et al. (1991) EMBO J. 10:2839-2848; Gearing, D. and Bruce, A. G. (1992) New. Biol. 4:61-65; and Schiemann, W. P. et al. (1995) Proc. Natl. Acad. Sci. USA 92:5361-5365. LIFR is also referred to in the art as Leukemia Inhibitor Factor Receptor Alpha, CD118, CD118 antigen, SJS2, STWS and SWS. A non-limiting example of a LILFR protein is the human protein having the amino acid sequence set forth in Genbank Accession Number NP_001121143.1.

As used herein, the terms “Fibroblast Growth Factor Receptor 3”, “FGF Receptor 3” and “FGFR3” are used interchangeably to refer to a protein known in the art that has been described in, for example, Keegan, K. et al. (1991) Proc. Natl. Acad. Sci. USA 88:1095-1099; Thompson, L. M. et al. (1991) Genomics 11:1133-1142; and Shiang, R. et al. (1994) Cell 78:335-343. FGFR3 is also referred to in the art as CD333, CD333 antigen, EC 2.7.10.1, JTK4, ACH, CEK2 and HSFGFR3EX. A non-limiting example of an FGFR3 protein is the human protein having the amino acid sequence set forth in Genbank Accession Number NP_000133.1.

As used herein, the term “stem cells” is used in a broad sense and includes traditional stem cells, progenitor cells, pre-progenitor cells, reserve cells, and the like. The term “stem cell” or “progenitor” are used interchangeably herein, and refer to an undifferentiated cell which is capable of proliferation and giving rise to more progenitor cells having the ability to generate a large number of mother cells that can in turn give rise to differentiated, or differentiable daughter cells. The daughter cells themselves can be induced to proliferate and produce progeny that subsequently differentiate into one or more mature cell types, while also retaining one or more cells with parental developmental potential. The term “stem cell” refers then, to a cell with the capacity or potential, under particular circumstances, to differentiate to a more specialized or differentiated phenotype, and which retains the capacity, under certain circumstances, to proliferate without substantially differentiating. In one embodiment, the term progenitor or stem cell refers to a generalized mother cell whose descendants (progeny) specialize, often in different directions, by differentiation, e.g., by acquiring completely individual characters, as occurs in progressive diversification of embryonic cells and tissues. Cellular differentiation is a complex process typically occurring through many cell divisions. A differentiated cell may derive from a multipotent cell which itself is derived from a multipotent cell, and so on. While each of these multipotent cells may be considered stem cells, the range of cell types each can give rise to may vary considerably. Some differentiated cells also have the capacity to give rise to cells of greater developmental potential. Such capacity may be natural or may be induced artificially upon treatment with various factors. In many biological instances, stem cells are also “multipotent” because they can produce progeny of more than one distinct cell type, but this is not required for “stem-ness.” Self-renewal is the other classical part of the stem cell definition, and it is essential as used in this document. In theory, self-renewal can occur by either of two major mechanisms. Stem cells may divide asymmetrically, with one daughter retaining the stem state and the other daughter expressing some distinct other specific function and phenotype. Alternatively, some of the stem cells in a population can divide symmetrically into two stems, thus maintaining some stem cells in the population as a whole, while other cells in the population give rise to differentiated progeny only. Formally, it is possible that cells that begin as stem cells might proceed toward a differentiated phenotype, but then “reverse” and re-express the stem cell phenotype, a term often referred to as “dedifferentiation”.

The term “progenitor cell” is used herein to refer to cells that have a cellular phenotype that is more primitive (e.g., is at an earlier step along a developmental pathway or progression than is a fully differentiated cell) relative to a cell which it can give rise to by differentiation. Often, progenitor cells also have significant or very high proliferative potential. Progenitor cells can give rise to multiple distinct differentiated cell types or to a single differentiated cell type, depending on the developmental pathway and on the environment in which the cells develop and differentiate.

The term “pluripotent” as used herein refers to a cell with the capacity, under different conditions, to differentiate to cell types characteristic of all three germ cell layers (endoderm, mesoderm and ectoderm). Pluripotent cells are characterized primarily by their ability to differentiate to all three germ layers, using, for example, a nude mouse and teratomas formation assay. Pluripotency is also evidenced by the expression of embryonic stem (ES) cell markers, although the preferred test for pluripotency is the demonstration of the capacity to differentiate into cells of each of the three germ layers. In some embodiments, a pluripotent cell is an undifferentiated cell.

The term “pluripotency” or a “pluripotent state” as used herein refers to a cell with the ability to differentiate into all three embryonic germ layers: endoderm (gut tissue), mesoderm (including blood, muscle, and vessels), and ectoderm (such as skin and nerve), and typically has the potential to divide in vitro for a long period of time, e.g., greater than one year or more than 30 passages.

The term “multipotent” when used in reference to a “multipotent cell” refers to a cell that is able to differentiate into some but not all of the cells derived from all three germ layers. Thus, a multipotent cell is a partially differentiated cell. Multipotent cells are well known in the art, and examples of multipotent cells include adult stem cells, such as for example, hematopoietic stem cells and neural stem cells. Multipotent means a stem cell may form many types of cells in a given lineage, but not cells of other lineages. For example, a multipotent blood stem cell can form the many different types of blood cells (red, white, platelets, etc.), but it cannot form neurons.

The term “embryonic stem cell” or “ES cell” or “ESC” are used interchangeably herein and refer to the pluripotent stem cells of the inner cell mass of the embryonic blastocyst (see U.S. Pat. Nos. 5,843,780, 6,200,806, which are incorporated herein by reference). Such cells can similarly be obtained from the inner cell mass of blastocysts derived from somatic cell nuclear transfer (see, for example, U.S. Pat. Nos. 5,945,577, 5,994,619, 6,235,970, which are incorporated herein by reference). The distinguishing characteristics of an embryonic stem cell define an embryonic stem cell phenotype. Accordingly, a cell has the phenotype of an embryonic stem cell if it possesses one or more of the unique characteristics of an embryonic stem cell such that that cell can be distinguished from other cells. Exemplary distinguishing embryonic stem cell characteristics include, without limitation, gene expression profile, proliferative capacity, differentiation capacity, karyotype, responsiveness to particular culture conditions, and the like. In some embodiments, an ES cell can be obtained without destroying the embryo, for example, without destroying a human embryo.

The term “adult stem cell” or “ASC” is used to refer to any multipotent stem cell derived from non-embryonic tissue, including fetal, juvenile, and adult tissue. Stem cells have been isolated from a wide variety of adult tissues including blood, bone marrow, brain, olfactory epithelium, skin, pancreas, skeletal muscle, and cardiac muscle. Each of these stem cells can be characterized based on gene expression, factor responsiveness, and morphology in culture.

Exemplary adult stem cells include neural stem cells, neural crest stem cells, mesenchymal stem cells, hematopoietic stem cells, and pancreatic stem cells. As indicated above, stem cells have been found resident in virtually every tissue. Accordingly, the present invention appreciates that stem cell populations can be isolated from virtually any animal tissue.

The term “human pluripotent stem cell” (abbreviated as hPSC), as used herein, refers to a human cell that has the capacity to differentiate into a variety of different cell types as discussed above regarding stem cells and pluripotency. Human pluripotent human stem cells include, for example, induced pluripotent stem cells (iPSC) and human embryonic stem cells, such as ES cell lines.

The term “human cardiac progenitor cell”, as used herein, refers to a human progenitor cell that is committed to the cardiac lineage and that has the capacity to differentiate into all three cardiac lineage cells (cardiac muscle cells, endothelial cells and smooth muscle cells).

The term “human cardiomyogenic progenitor cell”, as used herein, refers to a human progenitor cell that is committed to the cardiac lineage and that predominantly differentiates into cardiac muscle cells (i.e., more than 50% of the differentiated cells, preferably more than 60%, 70%, 80% or 90% of the differentiated cells, derived from the progenitor cells are cardiac muscle cells).

The term “cardiac ventricular progenitor cell”, as used herein, refers to a progenitor cell that is committed to the cardiac lineage and that predominantly differentiates into cardiac ventricular muscle cells (i.e., more than 50% of the differentiated cells, preferably more than 60%, 70%, 80% or 90% of the differentiated cells, derived from the progenitor cells are cardiac ventricular muscle cells). This type of cell is also referred to herein as a human ventricular progenitor, or HVP, cell.

The term “cardiomyocyte” refers to a muscle cell of the heart (e.g. a cardiac muscle cell). A cardiomyocyte will generally express on its cell surface and/or in the cytoplasm one or more cardiac-specific marker. Suitable cardiomyocyte-specific markers include, but are not limited to, cardiac troponin I, cardiac troponin-C, tropomyosin, caveolin-3, GATA-4, myosin heavy chain, myosin light chain-2a, myosin light chain-2v, ryanodine receptor, and atrial natriuretic factor.

The term “derived from” used in the context of a cell derived from another cell means that a cell has stemmed (e.g. changed from or produced by) a cell that is a different cell type. The term “derived from” also refers to cells that have been differentiated from a progenitor cell.

The term “Isl1+ cardiac progenitor cell”, as used herein, refers to a human progenitor cell that is committed to the cardiac lineage and that expresses Islet 1.

The term “Isl1+ JAG1+ cardiac progenitor cell”, as used herein, refers to a human progenitor cell that is committed to the cardiac lineage and that expresses both Islet 1 and Jagged 1.

The term “Isl1+ FZD4+ cardiac progenitor cell”, as used herein, refers to a human progenitor cell that is committed to the cardiac lineage and that expresses both Islet 1 and Frazzled 4.

The term “Isl1+ LIFR+ cardiac progenitor cell”, as used herein, refers to a human progenitor cell that is committed to the cardiac lineage and that expresses both Islet 1 and LIFR.

The term “Isl1+ FGFR3+ cardiac progenitor cell”, as used herein, refers to a human progenitor cell that is committed to the cardiac lineage and that expresses both Islet 1 and FGFR3.

The term “Isl1+ TNFSF9+ cardiac progenitor cell”, as used herein, refers to a human progenitor cell that is committed to the cardiac lineage and that expresses both Islet 1 and TNFSF9.

The term “Isl1+ JAG1+ FZD4+ LIFR+ FGFR3+ TNFSF9+ cardiac progenitor cell”, as used herein, refers to a human progenitor cell that is committed to the cardiac lineage and that expresses Islet 1, JAG1, FZD4, LIFR, FGFR3 and TNFSF9.

With respect to cells in cell cultures or in cell populations, the term “substantially free of” means that the specified cell type of which the cell culture or cell population is free, is present in an amount of less than about 10%, less than about 9%, less than about 8%, less than about 7%, less than about 6%, less than about 5%, less than about 4%, less than about 3%, less than about 2% or less than about 1% of the total number of cells present in the cell culture or cell population.

In the context of cell ontogeny, the adjective “differentiated”, or “differentiating” is a relative term. A “differentiated cell” is a cell that has progressed further down the developmental pathway than the cell it is being compared with. Thus, stem cells can differentiate to lineage-restricted precursor cells (such as a mesodermal stem cell), which in turn can differentiate into other types of precursor cells further down the pathway (such as an cardiomyocyte precursor), and then to an end-stage differentiated cell, which plays a characteristic role in a certain tissue type, and may or may not retain the capacity to proliferate further.

The term “differentiation” in the present context means the formation of cells expressing markers known to be associated with cells that are more specialized and closer to becoming terminally differentiated cells incapable of further differentiation. The pathway along which cells progress from a less committed cell, to a cell that is increasingly committed to a particular cell type, and eventually to a terminally differentiated cell is referred to as progressive differentiation or progressive commitment. Cell which are more specialized (e.g., have begun to progress along a path of progressive differentiation) but not yet terminally differentiated are referred to as partially differentiated. Differentiation is a developmental process whereby cells assume a specialized phenotype, e.g., acquire one or more characteristics or functions distinct from other cell types. In some cases, the differentiated phenotype refers to a cell phenotype that is at the mature endpoint in some developmental pathway (a so called terminally differentiated cell). In many, but not all tissues, the process of differentiation is coupled with exit from the cell cycle. In these cases, the terminally differentiated cells lose or greatly restrict their capacity to proliferate. However, we note that in the context of this specification, the terms “differentiation” or “differentiated” refer to cells that are more specialized in their fate or function than at a previous point in their development, and includes both cells that are terminally differentiated and cells that, although not terminally differentiated, are more specialized than at a previous point in their development. The development of a cell from an uncommitted cell (for example, a stem cell), to a cell with an increasing degree of commitment to a particular differentiated cell type, and finally to a terminally differentiated cell is known as progressive differentiation or progressive commitment. A cell that is “differentiated” relative to a progenitor cell has one or more phenotypic differences relative to that progenitor cell. Phenotypic differences include, but are not limited to morphologic differences and differences in gene expression and biological activity, including not only the presence or absence of an expressed marker, but also differences in the amount of a marker and differences in the co-expression patterns of a set of markers.

The term “differentiation” as used herein refers to the cellular development of a cell from a primitive stage towards a more mature (i.e. less primitive) cell.

As used herein, “proliferating” and “proliferation” refers to an increase in the number of cells in a population (growth) by means of cell division. Cell proliferation is generally understood to result from the coordinated activation of multiple signal transduction pathways in response to the environment, including growth factors and other mitogens. Cell proliferation may also be promoted by release from the actions of intra- or extracellular signals and mechanisms that block or negatively affect cell proliferation.

The terms “renewal” or “self-renewal” or “proliferation” are used interchangeably herein, and refers to a process of a cell making more copies of itself (e.g. duplication) of the cell. In some embodiments, cells are capable of renewal of themselves by dividing into the same undifferentiated cells (e.g. progenitor cell type) over long periods, and/or many months to years. In some instances, proliferation refers to the expansion of cells by the repeated division of single cells into two identical daughter cells.

The term “lineages” as used herein refers to a term to describe cells with a common ancestry or cells with a common developmental fate, for example cells that have a developmental fate to develop into ventricular cardiomyocytes.

The term “clonal population”, as used herein, refers to a population of cells that is derived from the outgrowth of a single cell. That is, the cells within the clonal population are all progeny of a single cell that was used to seed the clonal population.

The term “media” as referred to herein is a medium for maintaining a tissue or cell population, or culturing a cell population (e.g. “culture media”) containing nutrients that maintain cell viability and support proliferation. The cell culture medium may contain any of the following in an appropriate combination: salt(s), buffer(s), amino acids, glucose or other sugar(s), antibiotics, serum or serum replacement, and other components such as peptide growth factors, etc. Cell culture media ordinarily used for particular cell types are known to those skilled in the art.

The term “phenotype” refers to one or a number of total biological characteristics that define the cell or organism under a particular set of environmental conditions and factors, regardless of the actual genotype.

A “marker” as used herein describes the characteristics and/or phenotype of a cell. Markers can be used for selection of cells comprising characteristics of interest. Markers will vary with specific cells. Markers are characteristics, whether morphological, functional or biochemical (enzymatic) characteristics particular to a cell type, or molecules expressed by the cell type. Such markers can be proteins, for example a cell surface protein that possesses an epitope for antibodies or other binding molecules available in the art. A marker may consist of any molecule found in a cell including, but not limited to, DNA, RNA, mRNA, proteins (peptides and polypeptides), lipids, polysaccharides, nucleic acids and steroids. Examples of morphological characteristics or traits include, but are not limited to, shape, size, and nuclear to cytoplasmic ratio. Examples of functional characteristics or traits include, but are not limited to, the ability to adhere to particular substrates, ability to incorporate or exclude particular dyes, ability to migrate under particular conditions, and the ability to differentiate along particular lineages. Markers may be detected by any method available to one of skill in the art.

The term “isolated cell” as used herein refers to a cell that has been removed from an organism in which it was originally found or a descendant of such a cell. Optionally the cell has been cultured in vitro, e.g., in the presence of other cells. Optionally the cell is later introduced into a second organism or re-introduced into the organism from which it (or the cell from which it is descended) was isolated.

The term “isolated population” with respect to an isolated population of cells as used herein refers to a population of cells that has been removed and separated from a mixed or heterogeneous population of cells. In some embodiments, an isolated population is a substantially pure population of cells as compared to the heterogeneous population from which the cells were isolated or enriched from.

The term “substantially pure”, with respect to a particular cell population, refers to a population of cells that is at least about 75%, preferably at least about 85%, more preferably at least about 90%, and most preferably at least about 95% pure, with respect to the cells making up a total cell population.

The terms “subject” and “individual” are used interchangeably herein, and refer to an animal, for example a human, to whom cardiac ventricular progenitor cells as disclosed herein can be implanted into, for e.g. treatment, which in some embodiments encompasses prophylactic treatment or for a disease model, with methods and compositions described herein, is or are provided. For treatment of disease states that are specific for a specific animal such as a human subject, the term “subject” refers to that specific animal. The terms “non-human animals” and “non-human mammals” are used interchangeably herein, and include mammals such as rats, mice, rabbits, sheep, cats, dogs, cows, pigs, and non-human primates. The term “subject” also encompasses any vertebrate including but not limited to mammals, reptiles, amphibians and fish. However, advantageously, the subject is a mammal such as a human, or other mammals such as a domesticated mammal, e.g. dog, cat, horse, and the like, or production mammal, e.g. cow, sheep, pig, and the like are also encompassed in the term subject.

As used herein, the term “recipient” refers to a subject that will receive a transplanted organ, tissue or cell.

The term “three-dimensional matrix” or “scaffold” or “matrices” as used herein refers in the broad sense to a composition comprising a biocompatible matrix, scaffold, or the like. The three-dimensional matrix may be liquid, gel, semi-solid, or solid at 25° C. The three-dimensional matrix may be biodegradable or non-biodegradable. In some embodiments, the three-dimensional matrix is biocompatible, or bioresorbable or bioreplacable. Exemplary three-dimensional matrices include polymers and hydrogels comprising collagen, fibrin, chitosan, MATRIGEL™, polyethylene glycol, dextrans including chemically crosslinkable or photocrosslinkable dextrans, processed tissue matrix such as submucosal tissue and the like. In certain embodiments, the three-dimensional matrix comprises allogeneic components, autologous components, or both allogeneic components and autologous components. In certain embodiments, the three-dimensional matrix comprises synthetic or semi-synthetic materials. In certain embodiments, the three-dimensional matrix comprises a framework or support, such as a fibrin-derived scaffold.

As used herein, the terms “administering,” “introducing” and “transplanting” are used interchangeably and refer to the placement of cardiomyogenic progenitor cells and/or cardiomyocytes differentiated as described herein into a subject by a method or route which results in at least partial localization of the cells at a desired site. The cells can be administered by any appropriate route that results in delivery to a desired location in the subject where at least a portion of the cells remain viable. The period of viability of the cells after administration to a subject can be as short as a few hours, e.g. twenty-four hours, to a few days, to as long as several years.

The term “statistically significant” or “significantly” refers to statistical significance and generally means a two standard deviation (2SD) below normal, or lower, concentration of the marker. The term refers to statistical evidence that there is a difference. It is defined as the probability of making a decision to reject the null hypothesis when the null hypothesis is actually true. The decision is often made using the p-value. The term “substantially” or “predominantly” as used herein means a proportion of at least about 60%, or preferably at least about 70% or at least about 80%, or at least about 90%, at least about 95%, at least about 97% or at least about 99% or more, or any integer between 70% and 100%.

The term “disease” or “disorder” is used interchangeably herein, and refers to any alternation in state of the body or of some of the organs, interrupting or disturbing the performance of the functions and/or causing symptoms such as discomfort, dysfunction, distress, or even death to the person afflicted or those in contact with a person. A disease or disorder can also related to a distemper, ailing, ailment, malady, disorder, sickness, illness, complaint, indisposition or affection.

As used herein, the phrase “cardiovascular condition, disease or disorder” is intended to include all disorders characterized by insufficient, undesired or abnormal cardiac function, e.g. ischemic heart disease, hypertensive heart disease and pulmonary hypertensive heart disease, valvular disease, congenital heart disease and any condition which leads to congestive heart failure in a subject, particularly a human subject. Insufficient or abnormal cardiac function can be the result of disease, injury and/or aging. By way of background, a response to myocardial injury follows a well-defined path in which some cells die while others enter a state of hibernation where they are not yet dead but are dysfunctional. This is followed by infiltration of inflammatory cells, deposition of collagen as part of scarring, all of which happen in parallel with in-growth of new blood vessels and a degree of continued cell death. As used herein, the term “ischemia” refers to any localized tissue ischemia due to reduction of the inflow of blood. The term “myocardial ischemia” refers to circulatory disturbances caused by coronary atherosclerosis and/or inadequate oxygen supply to the myocardium. For example, an acute myocardial infarction represents an irreversible ischemic insult to myocardial tissue. This insult results in an occlusive (e.g., thrombotic or embolic) event in the coronary circulation and produces an environment in which the myocardial metabolic demands exceed the supply of oxygen to the myocardial tissue.

As used herein, the term “treating” or “treatment” are used interchangeably herein and refers to reducing or decreasing or alleviating or halting at least one adverse effect or symptom of a cardiovascular condition, disease or disorder, i.e., any disorder characterized by insufficient or undesired cardiac function. Adverse effects or symptoms of cardiac disorders are well-known in the art and include, but are not limited to, dyspnea, chest pain, palpitations, dizziness, syncope, edema, cyanosis, pallor, fatigue and death. In some embodiments, the term “treatment” as used herein refers to prophylactic treatment or preventative treatment to prevent the development of a symptom of a cardiovascular condition in a subject.

Treatment is generally “effective” if one or more symptoms or clinical markers are reduced as that term is defined herein. Alternatively, a treatment is “effective” if the progression of a disease is reduced or halted. That is, “treatment” includes not just the improvement of symptoms or decrease of markers of the disease, but also a cessation or slowing of progress or worsening of a symptom that would be expected in absence of treatment. Beneficial or desired clinical results include, but are not limited to, alleviation of one or more symptom(s), diminishment of extent of disease, stabilized (i.e., not worsening) state of disease, delay or slowing of disease progression, amelioration or palliation of the disease state, and remission (whether partial or total), whether detectable or undetectable. “Treatment” can also mean prolonging survival as compared to expected survival if not receiving treatment. Those in need of treatment include those already diagnosed with a cardiac condition, as well as those likely to develop a cardiac condition due to genetic susceptibility or other factors such as weight, diet and health. In some embodiments, the term to treat also encompasses preventative measures and/or prophylactic treatment, which includes administering a pharmaceutical composition as disclosed herein to prevent the onset of a disease or disorder.

A therapeutically significant reduction in a symptom is, e.g. at least about 10%, at least about 20%, at least about 30%, at least about 40%, at least about 50%, at least about 60%, at least about 70%, at least about 80%, at least about 90%, at least about 100%, at least about 125%, at least about 150% or more in a measured parameter as compared to a control or non-treated subject. Measured or measurable parameters include clinically detectable markers of disease, for example, elevated or depressed levels of a biological marker, as well as parameters related to a clinically accepted scale of symptoms or markers for a disease or disorder. It will be understood, that the total daily usage of the compositions and formulations as disclosed herein will be decided by the attending physician within the scope of sound medical judgment. The exact amount required will vary depending on factors such as the type of disease being treated.

With reference to the treatment of a cardiovascular condition or disease in a subject, the term “therapeutically effective amount” refers to the amount that is safe and sufficient to prevent or delay the development or a cardiovascular disease or disorder. The amount can thus cure or cause the cardiovascular disease or disorder to go into remission, slow the course of cardiovascular disease progression, slow or inhibit a symptom of a cardiovascular disease or disorder, slow or inhibit the establishment of secondary symptoms of a cardiovascular disease or disorder or inhibit the development of a secondary symptom of a cardiovascular disease or disorder. The effective amount for the treatment of the cardiovascular disease or disorder depends on the type of cardiovascular disease to be treated, the severity of the symptoms, the subject being treated, the age and general condition of the subject, the mode of administration and so forth. Thus, it is not possible to specify the exact “effective amount”. However, for any given case, an appropriate “effective amount” can be determined by one of ordinary skill in the art using only routine experimentation. The efficacy of treatment can be judged by an ordinarily skilled practitioner, for example, efficacy can be assessed in animal models of a cardiovascular disease or disorder as discussed herein, for example treatment of a rodent with acute myocardial infarction or ischemia-reperfusion injury, and any treatment or administration of the compositions or formulations that leads to a decrease of at least one symptom of the cardiovascular disease or disorder as disclosed herein, for example, increased heart ejection fraction, decreased rate of heart failure, decreased infarct size, decreased associated morbidity (pulmonary edema, renal failure, arrhythmias) improved exercise tolerance or other quality of life measures, and decreased mortality indicates effective treatment. In embodiments where the compositions are used for the treatment of a cardiovascular disease or disorder, the efficacy of the composition can be judged using an experimental animal model of cardiovascular disease, e.g., animal models of ischemia-reperfusion injury (Headrick J P, Am J Physiol Heart circ Physiol 285; H1797; 2003) and animal models acute myocardial infarction. (Yang Z, Am J Physiol Heart Circ. Physiol 282:H949:2002; Guo Y, J Mol Cell Cardiol 33; 825-830, 2001). When using an experimental animal model, efficacy of treatment is evidenced when a reduction in a symptom of the cardiovascular disease or disorder, for example, a reduction in one or more symptom of dyspnea, chest pain, palpitations, dizziness, syncope, edema, cyanosis, pallor, fatigue and high blood pressure which occurs earlier in treated, versus untreated animals. By “earlier” is meant that a decrease, for example in the size of the tumor occurs at least 5% earlier, but preferably more, e.g., one day earlier, two days earlier, 3 days earlier, or more.

As used herein, the term “treating” when used in reference to a treatment of a cardiovascular disease or disorder is used to refer to the reduction of a symptom and/or a biochemical marker of a cardiovascular disease or disorder, for example a reduction in at least one biochemical marker of a cardiovascular disease by at least about 10% would be considered an effective treatment. Examples of such biochemical markers of cardiovascular disease include a reduction of, for example, creatine phosphokinase (CPK), aspartate aminotransferase (AST), lactate dehydrogenase (LDH) in the blood, and/or a decrease in a symptom of cardiovascular disease and/or an improvement in blood flow and cardiac function as determined by someone of ordinary skill in the art as measured by electrocardiogram (ECG or EKG), or echocardiogram (heart ultrasound), Doppler ultrasound and nuclear medicine imaging. A reduction in a symptom of a cardiovascular disease by at least about 10% would also be considered effective treatment by the methods as disclosed herein. As alternative examples, a reduction in a symptom of cardiovascular disease, for example a reduction of at least one of the following; dyspnea, chest pain, palpitations, dizziness, syncope, edema, cyanosis etc. by at least about 10% or a cessation of such systems, or a reduction in the size one such symptom of a cardiovascular disease by at least about 10% would also be considered as affective treatments by the methods as disclosed herein. In some embodiments, it is preferred, but not required that the therapeutic agent actually eliminate the cardiovascular disease or disorder, rather just reduce a symptom to a manageable extent.

Subjects amenable to treatment by the methods as disclosed herein can be identified by any method to diagnose myocardial infarction (commonly referred to as a heart attack) commonly known by persons of ordinary skill in the art are amenable to treatment using the methods as disclosed herein, and such diagnostic methods include, for example but are not limited to; (i) blood tests to detect levels of creatine phosphokinase (CPK), aspartate aminotransferase (AST), lactate dehydrogenase (LDH) and other enzymes released during myocardial infarction; (ii) electrocardiogram (ECG or EKG) which is a graphic recordation of cardiac activity, either on paper or a computer monitor. An ECG can be beneficial in detecting disease and/or damage; (iii) echocardiogram (heart ultrasound) used to investigate congenital heart disease and assessing abnormalities of the heart wall, including functional abnormalities of the heart wall, valves and blood vessels; (iv) Doppler ultrasound can be used to measure blood flow across a heart valve; (v) nuclear medicine imaging (also referred to as radionuclide scanning in the art) allows visualization of the anatomy and function of an organ, and can be used to detect coronary artery disease, myocardial infarction, valve disease, heart transplant rejection, check the effectiveness of bypass surgery, or to select patients for angioplasty or coronary bypass graft.

The terms “coronary artery disease” and “acute coronary syndrome” as used interchangeably herein, and refer to myocardial infarction refer to a cardiovascular condition, disease or disorder, include all disorders characterized by insufficient, undesired or abnormal cardiac function, e.g. ischemic heart disease, hypertensive heart disease and pulmonary hypertensive heart disease, valvular disease, congenital heart disease and any condition which leads to congestive heart failure in a subject, particularly a human subject. Insufficient or abnormal cardiac function can be the result of disease, injury and/or aging. By way of background, a response to myocardial injury follows a well-defined path in which some cells die while others enter a state of hibernation where they are not yet dead but are dysfunctional. This is followed by infiltration of inflammatory cells, deposition of collagen as part of scarring, all of which happen in parallel with in-growth of new blood vessels and a degree of continued cell death.

As used herein, the term “ischemia” refers to any localized tissue ischemia due to reduction of the inflow of blood. The term “myocardial ischemia” refers to circulatory disturbances caused by coronary atherosclerosis and/or inadequate oxygen supply to the myocardium. For example, an acute myocardial infarction represents an irreversible ischemic insult to myocardial tissue. This insult results in an occlusive (e.g., thrombotic or embolic) event in the coronary circulation and produces an environment in which the myocardial metabolic demands exceed the supply of oxygen to the myocardial tissue.

The terms “composition” or “pharmaceutical composition” used interchangeably herein refer to compositions or formulations that usually comprise an excipient, such as a pharmaceutically acceptable carrier that is conventional in the art and that is suitable for administration to mammals, and preferably humans or human cells. In some embodiments, pharmaceutical compositions can be specifically formulated for direct delivery to a target tissue or organ, for example, by direct injection or via catheter injection to a target tissue. In other embodiments, compositions can be specifically formulated for administration via one or more of a number of routes, including but not limited to, oral, ocular parenteral, intravenous, intraarterial, subcutaneous, intranasal, sublingual, intraspinal, intracerebroventricular, and the like. In addition, compositions for topical (e.g., oral mucosa, respiratory mucosa) and/or oral administration can form solutions, suspensions, tablets, pills, capsules, sustained-release formulations, oral rinses, or powders, as known in the art are described herein. The compositions also can include stabilizers and preservatives. For examples of carriers, stabilizers and adjuvants, University of the Sciences in Philadelphia (2005) Remington: The Science and Practice of Pharmacy with Facts and Comparisons, 21st Ed.

As used herein, the terms “administering,” “introducing” and “transplanting” are used interchangeably and refer to the placement of a pharmaceutical composition comprising cardiomyogenic progenitor cells, or a composition comprising a population of differentiated cardiomyocytes (e.g., ventricular cardiomyocytes) as described herein, into a subject by a method or route which results in at least partial localization of the pharmaceutical composition, at a desired site or tissue location. In some embodiments, the pharmaceutical composition can be administered by any appropriate route which results in effective treatment in the subject, i.e. administration results in delivery to a desired location or tissue in the subject where at least a portion of the cells are located at a desired target tissue or target cell location.

The phrases “parenteral administration” and “administered parenterally” as used herein mean modes of administration other than enteral and topical administration, usually by injection, and includes, without limitation, intravenous, intramuscular, intraarterial, intrathecal, intraventricular, intracapsular, intraorbital, intracardiac, intradermal, intraperitoneal, transtracheal, subcutaneous, subcuticular, intraarticular, sub capsular, subarachnoid, intraspinal, intracerebro spinal, and intrasternal injection and infusion. The phrases “systemic administration,” “administered systemically”, “peripheral administration” and “administered peripherally” as used herein mean the administration of cardiovascular stem cells and/or their progeny and/or compound and/or other material other than directly into the cardiac tissue, such that it enters the animal's system and, thus, is subject to metabolism and other like processes, for example, subcutaneous or intravenous administration.

The phrase “pharmaceutically acceptable” is employed herein to refer to those compounds, materials, compositions, and/or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of human beings and animals without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio.

The phrase “pharmaceutically acceptable carrier” as used herein means a pharmaceutically acceptable material, composition or vehicle, such as a liquid or solid filler, diluent, excipient, solvent or encapsulating material, involved in carrying or transporting the subject agents from one organ, or portion of the body, to another organ, or portion of the body. Each carrier must be “acceptable” in the sense of being compatible with the other ingredients of the formulation.

The term “drug” or “compound” or “test compound” as used herein refers to a chemical entity or biological product, or combination of chemical entities or biological products, administered to a subject to treat or prevent or control a disease or condition. The chemical entity or biological product is preferably, but not necessarily a low molecular weight compound, but may also be a larger compound, for example, an oligomer of nucleic acids, amino acids, or carbohydrates including without limitation proteins, oligonucleotides, ribozymes, DNAzymes, glycoproteins, siRNAs, lipoproteins, aptamers, and modifications and combinations thereof.

The term “transplantation” as used herein refers to introduction of new cells (e.g. reprogrammed cells), tissues (such as differentiated cells produced from reprogrammed cells), or organs into a host (i.e. transplant recipient or transplant subject)

The terms “agent reactive with JAG1”, “agent reactive with FZD4”, “agent reactive with LIFR”, “agent that reacts with FGFR3” and “agent reactive with TNFSF9”, as used herein, refers to an agent that binds to or otherwise interacts with JAG1, FZD4, LIFR, FGFR3 or TNFSF9, respectively. Preferably, the agent “specifically” binds or otherwise interacts with JAG1, FZD4, LIFR, FGFR3 or TNFSF9, respectively, such that it does not bind or interact with other proteins.

The term “agent reactive with Islet 1”, as used herein, refers to an agent that binds to or otherwise interacts with Islet 1. Preferably, the agent “specifically” binds or otherwise interacts with Islet 1 such that it does not bind or interact with other non-Islet 1 proteins.

The term “antibody”, as used herein, includes whole antibodies and any antigen binding fragment (i.e., “antigen-binding portion”) or single chain thereof. An “antibody” refers, in one preferred embodiment, to a glycoprotein comprising at least two heavy (H) chains and two light (L) chains inter-connected by disulfide bonds, or an antigen binding portion thereof. Each heavy chain is comprised of a heavy chain variable region (abbreviated herein as V_(H)) and a heavy chain constant region. The heavy chain constant region is comprised of three domains, CH1, CH2 and CH3. Each light chain is comprised of a light chain variable region (abbreviated herein as V_(L)) and a light chain constant region. The light chain constant region is comprised of one domain, CL. The term “antigen-binding portion” of an antibody (or simply “antibody portion”), as used herein, refers to one or more fragments of an antibody that retain the ability to specifically bind to an antigen.

The term “monoclonal antibody,” as used herein, refers to an antibody that displays a single binding specificity and affinity for a particular epitope.

The term “human monoclonal antibody”, as used herein, refers to an antibody which displays a single binding specificity and which has variable and optional constant regions derived from human germline immunoglobulin sequences.

The term “humanized monoclonal antibody”, as used herein, refers to an antibody which displays a single binding specificity and which has heavy and light chain CDR1, 2 and 3 from a non-human antibody (e.g., a mouse monoclonal antibody) grafted into human framework and constant regions.

The term “chimeric monoclonal antibody”, as used herein, refers to an antibody which displays a single binding specificity and which has heavy and light chain variable regions from one species linked to constant regions from another species.

The term “fusion protein”, as used herein, refers to a composite protein, typically made using recombinant DNA technology, in which two different proteins, or portions thereof, are operatively linked together. A non-limiting example is an Fc fusion protein in which a non-immunoglobulin protein is operatively linked to an immunoglobulin Fc region.

Various aspects of the invention are described in further detail in the following subsections.

Methods of Identifying and Transplanting Engraftable Human Ventricular Progenitor Cells

It has been determined that engraftable HVPs typically develop between days 5-7 of differentiation (e.g., day 6) under the culture conditions described below and in Examples 1 and 11, express the intracellular marker Islet 1 and express cell surface markers including JAG1, FZD4, LIFR, FGFR3 and/or TNFSF9 (see e.g., U.S. Ser. No. 14/832,324, filed Aug. 21, 2015, and U.S. Ser. No. 14/984,783, filed Dec. 30, 2015, the entire contents of each of which are expressly incorporated herein by reference). To further characterize the gene expression profile of engraftable HVPs, RNA sequencing was performed at different time points on HVPs undergoing differentiation, as described in Examples 12 and 13. Cluster analysis of gene expression profiles at different time points was used to identify stage-specific signature genes. Gene ontogeny searches then allowed for the identification of genes (angiogenic family genes and extracellular matrix family genes) critical for cell engraftment, referred to herein as engraftment markers.

In one embodiment, the engraftment marker is an angiogenic marker. In a particular embodiment, the angiogenic marker is a positive angiogenic marker. Table 1 lists those angiogenic genes whose expression profile strongly correlates with Islet 1 (Isl1) expression in the HVPs (a Pearson correlation with Isl1 expression of 0.50 or greater). Table 2 lists additional angiogenic genes whose expression profile correlates with Isl1 expression in HVPs (a Pearson correlation with Isl1 expression between 0.49 and 0.00). In another particular embodiment, the angiogenic marker is a negative angiogenic marker. Table 3 lists those angiogenic genes whose expression profile strongly negatively correlates with Islet 1 (Isl1) expression in the HVPs (a Pearson correlation with Isl1 expression of −0.50 or less). Table 4 lists additional angiogenic genes whose expression profile negatively correlates with Isl1 expression in HVPs (a Pearson correlation with Isl1 expression between 0.00 and −0.49).

In one embodiment, the engraftment marker is an extracellular matrix marker. In a particular embodiment, the extracellular marker is a positive extracellular matrix marker. Table 5 lists those extracellular matrix genes whose expression profile strongly correlates with Islet 1 (Isl1) expression in the HVPs (a Pearson correlation with Isl1 expression of 0.50 or greater). Table 6 lists additional extracellular matrix genes whose expression profile correlates with Isl1 expression in HVPs (a Pearson correlation with Isl1 expression between 0.49 and 0.00). In another particular embodiment, the extracellular matrix marker is a negative extracellular matrix marker. Table 7 lists those extracellular matrix genes whose expression profile strongly negatively correlates with Islet 1 (Isl1) expression in the HVPs (a Pearson correlation with Isl1 expression of −0.50 or less). Table 8 lists additional extracellular matrix genes whose expression profile negatively correlates with Isl1 expression in HVPs (a Pearson correlation with Isl1 expression between 0.00 and −0.49).

Accordingly, in one aspect, the invention provides a method of identifying engraftable human ventricular progenitor cells (HVPs), the method comprising:

-   -   detecting expression of at least one engraftment marker in the         HVPs to thereby identify engraftable HVPs, wherein:     -   the HVPs also express at least one surface marker selected from         the group consisting of: JAG1, FZD4, LIFR, FGFR3 and/or TNFSF9.

In another embodiment, the invention provides a method of isolating engraftable human ventricular progenitor cells (HVPs), the method comprising:

-   -   culturing human cells containing cardiac progenitor cells under         conditions causing differentiation into human ventricular         progenitor cells (HVPs);     -   detecting expression on the HVPs of at least one surface marker         selected from the group consisting of JAG1, FZD4, LIFR, FGFR3         and/or TNFSF9;     -   detecting expression in the HVPs of at least one engraftment         marker; and     -   isolating HVPs that co-express the at least one surface marker         and the at least one engraftment marker to thereby isolate         engraftable HVPs.

In another embodiment, the invention provides a method for engrafting human ventricular tissue in a subject, the method comprising:

-   -   transplanting engraftable human ventricular progenitor cells         (HVPs) into the subject such that human ventricular tissue is         engrafted in the subject,     -   wherein prior to transplantation, engraftable HVPs are         identified by detecting expression of at least one engraftment         marker in the HVPs; and     -   wherein the HVPs express at least one surface marker selected         from the group consisting of: JAG1, FZD4, LIFR, FGFR3 and/or         TNFSF9.

In another embodiment, the invention provides a method for engrafting human ventricular tissue in a subject, the method comprising:

-   -   culturing human cells containing cardiac progenitor cells under         conditions causing differentiation into human ventricular         progenitor cells (HVPs);     -   detecting expression on the HVPs of at least one surface marker         selected from the group consisting of JAG1, FZD4, LIFR, FGFR3         and/or TNFSF9;     -   detecting expression in the HVPs of at least one engraftment         marker;     -   isolating HVPs that co-express the at least one surface marker         and the at least one engraftment marker to thereby isolate         engraftable HVPs; and     -   transplanting engraftable the HVPs into the subject such that         human ventricular tissue is engrafted in the subject.

In another embodiment, the invention provides a method for engrafting human ventricular tissue in a subject, the method comprising:

-   -   culturing human cells containing cardiac progenitor cells under         conditions causing differentiation into human ventricular         progenitor cells (HVPs) expressing at least one surface marker         selected from the group consisting of JAG1, FZD4, LIFR, FGFR3         and/or TNFSF9;     -   isolating the HVPs expressing the at least one surface marker to         form an HVP population;     -   detecting expression of at least one engraftment marker in a         sample of the HVP population; and     -   transplanting the HVPs expressing the at least one surface         marker and the at least one engraftment marker into the subject         such that human ventricular tissue is engrafted in the subject.

In another embodiment, the invention provides a method for engrafting human ventricular tissue in a subject, the method comprising:

-   -   contacting a culture of human cells containing human ventricular         progenitor cells (HVPs) with at least one agent reactive with at         least one surface marker selected from the group consisting of         JAG1, FZD4, LIFR, FGFR3 and/or TNFSF9 such that a population of         HVPs is isolated;     -   expanding a clonal population of HVPs from the isolated         population of HVPs;     -   detecting expression of at least one engraftment marker in a         sample of the clonal population of HVPs; and     -   transplanting the clonal population of HVPs expressing the at         least one surface marker and the at least one engraftment marker         into the subject such that human ventricular tissue is engrafted         in the subject.

In one embodiment, the at least one engraftment marker detected is at least one positive angiogenic marker. More than one positive angiogenic marker can be detected, for example, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more, fifteen or more, or twenty or more positive angiogenic markers can be detected.

In another embodiment, the at least one engraftment marker detected is at least one positive extracellular matrix marker. More than one positive extracellular marker can be detected, for example, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more, fifteen or more, or twenty or more positive extracellular markers can be detected.

In another embodiment, the at least one engraftment marker detected is at least one positive angiogenic marker and at least one positive extracellular matrix marker. More than one of each positive marker (angiogenic and extracellular matrix) can be detected, for example, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more, fifteen or more, or twenty or more positive angiogenic and extracellular markers each can be detected.

In one embodiment, the at least one positive angiogenic marker is selected from the group consisting of: FGF10, PRKD1, CCBE1, PDGFRA, EPHB2, GATA2, NTRK1, PTGIS, BMPER, BMP4, C1GALT1, MEIS1, TBX1, PKNOX1, ID1, TCF21, HEY1, HOXB3, HGF, IL6, GHRL, IHH, SRPK2, GATA6, HAND1, AMOT, NRP2, PTEN, SEMA3E, APOLD1, SETD2, DAB2IP, KDR, PGF, EMP2, TAL1, ACVR1, HIPK2, CSPG4, TNFAIP3, NRP1, NFATC4, CDC42, ANGPTL4, BCAS3, HIPK1, NRXN3, FZD5 and HHEX. In another embodiment, the at least one positive angiogenic marker is selected from the group consisting of: FGF10, PRKD1, CCBE1, PDGFRA, EPHB2, GATA2, NTRK1, PTGIS, BMPER, BMP4, C1GALT1, MEIS1, TBX1, PKNOX1, ID1, TCF21 and HEY1. In another embodiment, the at least positive angiogenic marker is selected from the group consisting of: FGF10, PRKD1, CCBE1, PDGFRA, EPHB2, GATA2 and NTRK1. In another embodiment, the positive angiogenic marker is FGF10. In another embodiment, the positive angiogenic marker is PRKD1. In another embodiment, the positive angiogenic marker is CCBE1. In another embodiment, the positive angiogenic marker is PDGFRA. In another embodiment, the positive angiogenic marker is EPHB2. In another embodiment, the positive angiogenic marker is GATA2. In another embodiment, the positive angiogenic marker is NTRK1. In another embodiment, the positive angiogenic marker is PTGIS. In another embodiment, the positive angiogenic marker is BMPER. In another embodiment, the positive angiogenic marker is BMP4.

In another embodiment, the at least one positive extracellular matrix marker is selected from the group consisting of: FGF10, SMOC1, CCBE1, COL6A6, ADAMTS12, COL19A1, LAMA1, BMP4, FBLN7, FBLN2, NDNF, HTRA1, HAPLN1, EMILIN1, SPOCK3, PODNL1, IHH, ACAN, NID2, COL4A6, LAMC1, FMOD, MUC4, EMID1, HMCN1, NID1, VCAN, CILP2, SOD3, ADAMTS3, ZP3, ANGPTL4, CRTAC1, LTBP4 and FREM1. In another embodiment, the at least one positive extracellular matrix marker is selected from the group consisting of: FGF10, SMOC1, CCBE1, COL6A6, ADAMTS12, COL19A1, LAMA1, BMP4, FBLN7, FBLN2, NDNF and HTRA1. In another embodiment, the at least one positive extracellular matrix marker is selected from the group consisting of: FGF10, SMOC1 and CCBE1. In another embodiment, the positive extracellular marker is FGF10. In another embodiment, the positive extracellular marker is SMOC1. In another embodiment, the positive extracellular marker is CCBE1. In another embodiment, the positive extracellular marker is COL6A6. In another embodiment, the positive extracellular marker is ADAMTS12. In another embodiment, the positive extracellular marker is COL19A1. In another embodiment, the positive extracellular marker is LAMA1. In another embodiment, the positive extracellular marker is BMP4. In another embodiment, the positive extracellular marker is FBLN7. In another embodiment, the positive extracellular marker is FBLN2.

In those embodiments in which both at least one positive angiogenic marker and at least one positive extracellular matrix marker are detected, the at least one positive angiogenic marker can be selected from the group consisting of: FGF10, PRKD1, CCBE1, PDGFRA, EPHB2, GATA2, NTRK1, PTGIS, BMPER, BMP4, C1GALT1, MEIS1, TBX1, PKNOX1, ID1, TCF21, HEY1, HOXB3, HGF, IL6, GHRL, IHH, SRPK2, GATA6, HAND1, AMOT, NRP2, PTEN, SEMA3E, APOLD1, SETD2, DAB2IP, KDR, PGF, EMP2, TAL1, ACVR1, HIPK2, CSPG4, TNFAIP3, NRP1, NFATC4, CDC42, ANGPTL4, BCAS3, HIPK1, NRXN3, FZD5 and HHEX; and

the at least one positive extracellular matrix marker can be selected from the group consisting of: FGF10, SMOC1, CCBE1, COL6A6, ADAMTS12, COL19A1, LAMA1, BMP4, FBLN7, FBLN2, NDNF, HTRA1, HAPLN1, EMILIN1, SPOCK3, PODNL1, IHH, ALAN, NID2, COL4A6, LAMC1, FMOD, MUC4, EMID1, HMCN1, NID1, VCAN, CILP2, SODS, ADAMTS3, ZP3, ANGPTL4, CRTAC1, LTBP4 and FREM1.

In another embodiment, the at least one positive angiogenic marker is selected from the group consisting of: FGF10, PRKD1, CCBE1, PDGFRA, EPHB2, GATA2, NTRK1, PTGIS, BMPER, BMP4, C1GALT1, MEIS1, TBX1, PKNOX1, ID1, TCF21 and HEY1; and the at least one positive extracellular matrix marker is selected from the group consisting of: FGF10, SMOC1, CCBE1, COL6A6, ADAMTS12, COL19A1, LAMA1, BMP4, FBLN7, FBLN2, NDNF and HTRA1.

In another embodiment, the at least one positive angiogenic marker is selected from the group consisting of: FGF10, PRKD1, CCBE1, PDGFRA, EPHB2, GATA2 and NTRK1; and the at least one positive extracellular matrix marker is selected from the group consisting of: FGF10, SMOC1 and CCBE1.

In one embodiment, the at least one engraftment marker detected is at least one negative angiogenic marker. More than one negative angiogenic marker can be detected, for example, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more, fifteen or more, or twenty or more negative angiogenic markers can be detected.

In another embodiment, the at least one engraftment marker detected is at least one negative extracellular matrix marker. More than one negative extracellular matrix marker can be detected, for example, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more, fifteen or more, or twenty or more negative extracellular matrix markers can be detected.

In another embodiment, the at least one engraftment marker detected is at least one negative angiogenic marker and at least one negative extracellular matrix marker. More than one of each negative marker (angiogenic and extracellular matrix) can be detected, for example, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more, fifteen or more, or twenty or more negative angiogenic and extracellular matrix markers each can be detected.

In one embodiment, the at least one negative angiogenic marker is selected from the group consisting of: ETS1, BAX, XBP1, TDGF1, C5AR1, EPHA1, HS6ST1, SHC1, SP100, JAM3, CASP8, FLT4, SFRP2, HPSE, BAK1, GPX1, VAV3, VAV2, EGF, ADAM15 and AGGF1. In another embodiment, the at least one negative angiogenic marker is selected from the group consisting of: VAV3, VAV2, EGF, ADAM15 and AGGF1.

In another embodiment, the at least one negative extracellular matrix marker is selected from the group consisting of: FKBP1A, CLU, TFP12, PLSCR1, FBLN5, VWA1, ADAMTS16, MMP25, SFRP2 and SOD1.

In those embodiments in which both at least one negative angiogenic marker and at least one negative extracellular matrix marker are detected, the at least one negative angiogenic marker can be selected from the group consisting of: ETS1, BAX, XBP1, TDGF1, C5AR1, EPHA1, HS6ST1, SHC1, SP100, JAM3, CASP8, FLT4, SFRP2, HPSE, BAK1, GPX1, VAV3, VAV2, EGF, ADAM15 and AGGF1; and

the at least one negative extracellular matrix marker can be selected from the group consisting of: FKBP1A, CLU, TFP12, PLSCR1, FBLN5, VWA1, ADAMTS16, MMP25, SFRP2 and SOD1.

The ordinarily skilled artisan will appreciate that the engraftment markers of the invention can be detected by any suitable method of detection known in the art for detecting nucleic acid or protein expression. Typically, mRNA encoding the engraftment marker(s) is detected, either directly or indirectly (e.g., by detection of cDNA prepared from the mRNA). Methods for detecting mRNAs or cDNAs are well established in the art, including but not limited to hybridization techniques, polymerase chain reaction, quantitative PCR, real-time quantitative PCR, RNA sequencing and the like. Methods for detecting protein expression also are well established in the art, including but not limited to western blotting, immunoprecipitation, immunohistochemistry, ELISA and the like. Accordingly, in one embodiment, to “detect” expression of an engraftment marker(s) in a population of HVPs, a sample of HVPs is taken from the population of HVPs, nucleic acid (e.g., mRNA, cDNA) is prepared from the sample and contacted with, for example, one or more pairs of oligonucleotide primers capable of amplifying nucleic acid encoding the engraftment marker(s) of interest, following by carrying out a PCR-type reaction (e.g., standard PCR, quantitative PCR, real-time Q-PCR) on the nucleic acid sample. Alternatively, the nucleic acid sample prepared from the population of HVPs can be contacted with one or more hybridization probes capable of binding to nucleic acid encoding the engraftment marker(s) of interest, followed by carrying out a hybridization reaction on the sample (e.g., northern blotting, southern blotting etc.). In another embodiment, to “detect” expression of an engraftment marker(s) in a population of HVPs, a sample of HVPs is taken from the population of HVPs, protein is prepared from the sample and contacted with, for example, one or more monoclonal antibodies that specifically bind to the engraftment marker(s) of interest, followed by carrying out an immunodetection method (e.g., western blotting, immunoprecipitation, ELISA etc.).

Suitable methods for determining the level of engraftment marker expression at the mRNA level include RNA sequencing, conventional microarray analysis, polymerase chain reaction (PCR), quantitative polymerase chain reaction (Q-PCR) and real-time quantitative PCR (RT-QPCR). In some embodiments, RNA is extracted from the HVPs using standard protocols. In other embodiments, RNA analysis is performed using techniques that do not require RNA isolation.

Methods for rapid and efficient extraction of eukaryotic mRNA, i.e., poly(a) RNA, from tissue samples are well established and known to those of skill in the art. See, e.g., Ausubel et al., 1997, Current Protocols of Molecular Biology, John Wiley & Sons. The use of commercially available kits with vendor's instructions for RNA extraction and preparation is widespread and common. Commercial vendors of various RNA isolation products and complete kits include Qiagen (Valencia, Calif.), Invitrogen (Carlsbad, Calif.), Ambion (Austin, Tex.) and Exiqon (Woburn, Mass.).

In general, RNA isolation begins with cell disruption. During cell disruption it is desirable to minimize RNA degradation by RNases. One approach to limiting RNase activity during the RNA isolation process is to ensure that a denaturant is in contact with cellular contents as soon as the cells are disrupted. Another common practice is to include one or more proteases in the RNA isolation process. Optionally, fresh tissue samples are immersed in an RNA stabilization solution, at room temperature, as soon as they are collected. The stabilization solution rapidly permeates the cells, stabilizing the RNA for storage at 4° C., for subsequent isolation. One such stabilization solution is available commercially as RNAlater® (Ambion, Austin, Tex.).

In some protocols, total RNA is isolated from disrupted cells by cesium chloride density gradient centrifugation. In general, mRNA makes up approximately 1% to 5% of total cellular RNA. Immobilized Oligo(dT), e.g., oligo(dT) cellulose, is commonly used to separate mRNA from ribosomal RNA and transfer RNA. If stored after isolation, RNA must be stored under RNase-free conditions. Methods for stable storage of isolated RNA are known in the art. Various commercial products for stable storage of RNA are available.

The mRNA expression level of engraftment markers can be measured using conventional DNA microarray expression profiling technology. A DNA microarray is a collection of specific DNA segments or probes affixed to a solid surface or substrate such as glass, plastic or silicon, with each specific DNA segment occupying a known location in the array. Hybridization with a sample of labeled RNA, usually under stringent hybridization conditions, allows detection and quantitation of RNA molecules corresponding to each probe in the array. After stringent washing to remove non-specifically bound sample material, the microarray is scanned by confocal laser microscopy or other suitable detection method. Modern commercial DNA microarrays, often known as DNA chips, typically contain tens of thousands of probes, and thus can measure expression of tens of thousands of genes simultaneously. Such microarrays can be used in practicing the present invention. Alternatively, custom chips containing as few probes as those needed to measure engraftment markers of interest, plus necessary controls or standards, e.g., for data normalization, can be used in practicing the disclosed methods.

To facilitate data normalization, a two-color microarray reader can be used. In a two-color (two-channel) system, samples are labeled with a first fluorophore that emits at a first wavelength, while an RNA or cDNA standard is labeled with a second fluorophore that emits at a different wavelength. For example, Cy3 (570 nm) and Cy5 (670 nm) often are employed together in two-color microarray systems.

DNA microarray technology is well-developed, commercially available, and widely employed. Therefore, in performing disclosed methods, a person of ordinary skill in the art can use microarray technology to measure expression levels of genes encoding engraftment markers without undue experimentation. DNA microarray chips, reagents (such as those for RNA or cDNA preparation, RNA or cDNA labeling, hybridization and washing solutions), instruments (such as microarray readers) and protocols are well known in the art and available from various commercial sources. Commercial vendors of microarray systems include Agilent Technologies (Santa Clara, Calif.) and Affymetrix (Santa Clara, Calif.), but other PCR systems can be used.

The level of mRNA encoding an engraftment marker(s) can be measured using conventional quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) technology. Advantages of qRT-PCR include sensitivity, flexibility, quantitative accuracy, and ability to discriminate between closely related mRNAs. Guidance concerning the processing of tissue samples for quantitative PCR is available from various sources, including manufacturers and vendors of commercial instruments and reagents for qRT-PCR (e.g., Qiagen (Valencia, Calif.) and Ambion (Austin, Tex.)). Instruments and systems for automated performance of qRT-PCR are commercially available and used routinely in many laboratories. An example of a well-known commercial system is the Applied Biosystems 7900HT Fast Real-Time PCR System (Applied Biosystems, Foster City, Calif.).

Once mRNA is isolated, the first step in gene expression measurement by RT-PCR is the reverse transcription of the mRNA template into cDNA, which is then exponentially amplified in a PCR reaction. Two commonly used reverse transcriptases are avilo myeloblastosis virus reverse transcriptase (AMV-RT) and Moloney murine leukemia virus reverse transcriptase (MMLV-RT). The reverse transcription reaction typically is primed with specific primers, random hexamers, or oligo(dT) primers. Suitable primers are commercially available, e.g., GeneAmp® RNA PCR kit (Perkin Elmer, Waltham, Mass.). The resulting cDNA product can be used as a template in the subsequent polymerase chain reaction.

The PCR step is carried out using a thermostable DNA-dependent DNA polymerase. The polymerase most commonly used in PCR systems is a Thermus aquaticus (Taq) polymerase. The selectivity of PCR results from the use of primers that are complementary to the DNA region targeted for amplification, i.e., regions of the cDNAs reverse transcribed from genes encoding proteins of interest. Therefore, when qRT-PCR is employed in the present invention, primers specific to each engraftment marker gene are based on the cDNA sequence of the gene. Commercial technologies such as SYBR® Green or TagMan® (Applied Biosystems, Foster City, Calif.) can be used in accordance with the vendor's instructions. Messenger RNA levels can be normalized for differences in loading among samples by comparing the levels of housekeeping genes such as beta-actin or GAPDH. The level of mRNA expression can be expressed relative to any single control sample, or a pool of control samples or a commercially available set of control mRNA.

Suitable primer sets for PCR analysis of expression of engraftment marker genes can be designed and synthesized by one of skill in the art, without undue experimentation. Alternatively, PCR primer sets for practicing the present invention can be purchased from commercial sources, e.g., Applied Biosystems. PCR primers preferably are about 17 to 25 nucleotides in length. Primers can be designed to have a particular melting temperature (Tm), using conventional algorithms for Tm estimation. Software for primer design and Tm estimation are available commercially, e.g., Primer Express™ (Applied Biosystems), and also are available on the internet, e.g., Primer3 (Massachusetts Institute of Technology). By applying established principles of PCR primer design, a large number of different primers can be used to measure the expression level of any given engraftment marker gene.

In some embodiments, RNA analysis is performed using a technology that does not involve RNA extraction or isolation. One such technology is quantitative nuclease protection assay, which is commercially available under the name gNPA™ (High Throughput Genomics, Inc., Tucson, Ariz.).

The methods of the invention encompass “detecting expression” of positive engraftment markers as well as negative engraftment markers. In those embodiments involving detecting positive engraftment markers (whose expression positively correlates with the expression of other HVP markers, such as Isl1), “detecting expression” of the at least one positive engraftment marker comprises detecting expression of mRNA encoding the at least one engraftment marker in the HVPs (detection of “positive” marker expression, such as a positive angiogenic marker(s) and/or a positive extracellular matrix marker(s)). Detecting expression of mRNA encoding the positive engraftment marker(s) is intended to encompass direct assaying of the mRNA as well as indirect assaying of the mRNA, such as by assaying of cDNA prepared from the mRNA.

In those embodiments involving detecting negative engraftment markers (whose expression negatively correlates with the expression of other HVP markers, such as Isl1), “detecting expression” of the at least one negative engraftment marker comprises detecting lack of expression of mRNA encoding the at least one engraftment marker in the HVPs (detection of lack of expression of “negative” markers, such as a negative angiogenic marker(s) and/or a negative extracellular matrix marker(s)). Detecting lack of expression of mRNA encoding the negative engraftment marker(s) is intended to encompass direct assaying of the mRNA as well as indirect assaying of the mRNA, such as by assaying of cDNA prepared from the mRNA. Furthermore, as used herein, “lack of expression” of an mRNA (e.g., an mRNA for a negative marker) is intended to mean that the Pearson correlation index of expression relative to expression of a positive HVP marker, such as Islet 1, JAG1, FZD4, LIFR, FGFR3 and/or TNFSF9, is about −0.50 or less.

In certain embodiments, the methods of the invention can comprise (i) detecting expression of at least one positive engraftment marker (e.g., positive angiogenic marker(s) and/or positive extracellular matrix marker(s)); and (ii) detecting lack of expression of at least one negative engraftment marker (e.g., negative angiogenic marker(s) and/or negative extracellular matrix marker(s)). For example, in one embodiment, the invention provides a method for engrafting human ventricular tissue in a subject, the method comprising:

-   -   culturing human cells containing cardiac progenitor cells under         conditions causing differentiation into human ventricular         progenitor cells (HVPs) expressing at least one surface marker         selected from the group consisting of JAG1, FZD4, LIFR, FGFR3         and/or TNFSF9;     -   isolating the HVPs expressing the at least one surface marker to         form an HVP population;     -   detecting expression of at least one positive engraftment marker         in a sample of the HVP population;     -   detecting lack of expression of at least one negative         engraftment marker in the sample of the HVP population; and     -   transplanting the HVPs expressing the at least one surface         marker and the at least one positive engraftment marker, and         lacking expression of the at least one negative engraftment         marker, into the subject such that human ventricular tissue is         engrafted in the subject.

Likewise, the other methods of the invention described above can similarly comprise the combination of: (i) detection of at least one positive engraftment marker (e.g., positive angiogenic marker(s) and/or positive extracellular matrix marker(s)); and (ii) detection of lack of expression of at least one negative engraftment marker (e.g., negative angiogenic marker(s) and/or negative extracellular matrix marker(s)).

As described in detail in Example 14, gene expression profiling has also been performed on the Islet 1 negative (Isl1−) subpopulation of cells within the Day 6 HVP population to thereby further characterize the Isl1− subpopulation of Day 6 progenitor cells that are not suitable for transplantation and engraftment. These studies determined that the Isl1− Day 6 subpopulation of cells express the following genes at significant levels (average of 2000 copies or more of mRNA): ACTB, MTRNR2L2, MALAT1, EEF1A1, KRT8, MTRNR2L8, KRT18, FN1, MTRNR2L1, TTN, GAPDH, YWHAZ, MTRNR2L9, RPL3, AHNAK, KCNQ1OT1, TUBB, SLC2A3, FTL, HSP90B1, KRT19, HSPA8, MYL6, RPLP0, BSG, COL3A1, TPM1, VCAN, ENO1, RPL4, ACTG1, MTRNR2L10, HMGN2, PRTG, TPI1, HMGB1, VIM, ATP5B, HSP90AB1, RPL7, CBX5, MYL7, SERPINH1, HNRNPK, SRRM2, PODXL, EEF2, SPARC, ACTC1, HUWE1, COL1A2, LINC00506, HSPA5, MDK, HNRNPC, HSP90AA1, RGS5, LAMC1, APLNR, UGDH-AS1 and RPS3A. This Isl1− Day 6 subpopulation of cells express the following genes at high levels (average of 5000 copies or more of mRNA): ACTB, MTRNR2L2, MALAT1, EEF1A1, KRT8, MTRNR2L8, KRT18, FN1, MTRNR2L1, TTN, GAPDH and YWHAZ.

Accordingly, this gene expression profile information for the Isl1− Day 6 subpopulation allows for further refinement of the selection process for choosing engraftable HVPs for transplantation. In particular, cells within a differentiated (e.g., day 5-7) culture of cardiac progenitor cells (e.g., cultured as described below and in Examples 1 and 11) can be analyzed for their gene expression profile and those cells that lack expression of Islet 1 (Isl1-) but that do express at least one marker selected from ACTB, MTRNR2L2, MALAT1, EEF1A1, KRT8, MTRNR2L8, KRT18, FN1, MTRNR2L1, TTN, GAPDH, YWHAZ, MTRNR2L9, RPL3, AHNAK, KCNQ1OT1, TUBB, SLC2A3, FTL, HSP90B1, KRT19, HSPA8, MYL6, RPLP0, BSG, COL3A1, TPM1, VCAN, ENO1, RPL4, ACTG1, MTRNR2L10, HMGN2, PRTG, TPI1, HMGB1, VIM, ATP5B, HSP90AB1, RPL7, CBX5, MYL7, SERPINH1, HNRNPK, SRRM2, PODXL, EEF2, SPARC, ACTC1, HUWE1, COL1A2, LINC00506, HSPA5, MDK, HNRNPC, HSP90AA1, RGS5, LAMC1, APLNR, UGDH-AS1 and RPS3A, can be ruled out for transplantation. Alternatively, cells that lack expression of Islet 1 (Isl1−) but that do express at least one marker selected from ACTB, MTRNR2L2, MALAT1, EEF1A1, KRT8, MTRNR2L8, KRT18, FN1, MTRNR2L1, TTN, GAPDH and YWHAZ can be ruled out for transplantation. In certain embodiments, cells ruled out for transplantation are Isl1− and express two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more, fifteen or more or twenty or more of the aforementioned markers.

Generation of Human Ventricular Progenitors (HVPs)

Human pluripotent stem cells can be cultured under conditions that lead to the generation of a non-clonal population of human ventricular progenitor cells. Culture conditions for generating cardiac progenitor cells have been described in the art (see e.g., Lian, X. et al. (2012) Proc. Natl. Acad. Sci. USA 109:E1848-1857; U.S. Patent Publication No. 20130189785) and also are described in detail in Example 1 and the drawing, as well as in Example 11. Typically, Wnt/β-catenin signaling is first activated in the hPSCs, followed by an incubation period, followed by inhibition of Wnt/β-catenin signaling.

Activation of Wnt/β-catenin signaling is achieved by incubation with a Gsk3 inhibitor, preferably CHIR98014 (CAS 556813-39-9). Inhibition of Wnt/β-catenin signaling is achieved by incubation with a Porcn inhibitor, preferably Wnt-059 (CAS 1243243-89-1). The Gsk3 inhibitor is used to promote cardiac mesodermal differentiation, whereas the Porcn inhibitor is used to enhance ventricular progenitor differentiation from mesoderm cells. With regard to timing of the use of the Gsk3 and Porcn inhibitors, typically, at day 0 of culture, the hPSCs are cultured with the Gsk3 inhibitor, at day 3 of culture the medium is changed to remove the Gsk3 inhibitor and the cells are then cultured with media containing the Porcn inhibitor through day 5 of culture. HVP generation is optimal between days 5 and 7 (inclusive) in culture and peaks at day 6 of culture. Other non-limiting, exemplary details on culture conditions and timing of the use of the Gsk3 and Porcn inhibitors are described in detail in Examples 1 and 11.

Suitable hPSCs for use in the methods of the invention include induced pluripotent stem cells (iPSC), such as 19-11-1, 19-9-7 or 6-9-9 cells (Yu, J. et al. (2009) Science 324:797-801), and human embryonic stem cell lines, such as ES03 cells (WiCell Research Institute) or H9 cells (Thomson, J. A. et al. (1998) Science 282:1145-1147). Suitable culture media for generating cardiomyogenic progenitors include E8 medium, mTeSR1 medium and RPMI/B27 minus insulin, each described further in Example 1 and/or Example 11.

Culture conditions have now been determined that bias the cardiomyogenic progenitor cells to the ventricular lineage. These ventricular cardiomyogenic progenitor cells can be cultured in RPMI/B27 medium and they can further differentiate into ventricular muscle cells. A preferred medium for culturing the cardiac ventricular progenitor cells in vitro such that they differentiation into ventricular cells in vitro (e.g., expressing the MLC2v marker described below) is the Cardiac Progenitor Culture (CPC) medium (advanced DMEM/F12 supplemented with 20% KnockOut Serum Replacement, 2.5 mM GlutaMAX and 100 μg/ml Vitamin C).

Known markers of differentiated cardiac cells can be used to identify the type(s) of cells that are generated by differentiation of the cardiac progenitor cells. For example, cardiac troponin I (cTnI) can be used as a marker of cardiomyocyte differentiation. CD144 (VE-cadherin) can be used as a marker of endothelial cells. Smooth muscle actin (SMA) can be used as a marker of smooth muscle cells. MLC2v can be used as a marker of ventricular muscle cells. MLC2a, which is expressed on both immature ventricular muscle cells and atrial muscle cells, can be used as a marker for those cell types. Additionally, sarcolipin, which is specifically expressed in atrial muscle cells, can be used as a marker for atrial muscle cells. Phospholamban, which is expressed predominantly in the ventricles and, to a lesser extent, in the atria, can also be used as a marker. Hairy-related transcription factor 1 (HRT1), also called Hey1, which is expressed in atrial cardiomyocytes, can be used as a marker for atrial cardiomyocytes. HRT2 (Hey2), which is expressed in ventricular cardiomyocytes, can be used as a marker for ventricular cardiomyocytes. In addition, IRX4 has a ventricular-restricted expression pattern during all stages of development, and thus can be used as a ventricular lineage marker. In summary, the genes expressed in the ventricles, and thus which are appropriate ventricular markers, are: MLC2v, IRX4 and HRT2, while genes expressed in the atria, and thus which are appropriate atrial markers are: MLC2a, HRT1, Sarcolipin and ANF (atrial natriuretic factor). The preferred marker of ventricular differentiation is MLC2v.

Methods of Isolating Human Cardiac Ventricular Progenitor Cells

Methods of isolating HVPs based on cell surface marker expression (e.g., JAG1, FZD4, LIFR, FGFR3 and/or TNFSF9) is described in detail in U.S. Ser. No. 14/832,324, filed Aug. 21, 2015, and U.S. Ser. No. 14/984,783, filed Dec. 30, 2015, the entire contents of each of which are expressly incorporated herein by reference). In brief, agents reactive with the cell surface marker are used to isolate the HVPs according to procedures well established in the art. Identification of JAG1, FZD4, LIFR and FGFR3 as cell surface markers of HVPs is also described in detail in Examples 2, 4 and 5.

In one embodiment, the agent reactive with the cell surface marker is an antibody that specifically binds to the cell surface marker, such as a monoclonal antibody. Non-limiting examples include murine, rabbit, human, humanized or chimeric monoclonal antibodies with binding specificity for the cells surface marker (e.g., anti-JAG1, anti-FZD4, anti-LIFR, anti-FGFR3 and/or anti-TNFSF9 antibodies). Such monoclonal antibodies are commercially available in the art (e.g., R&D Systems, Santa Cruz Biotechnology). Moreover, such antibodies can be prepared using standard techniques well established in the art using the cell surface marker as the antigen.

In another embodiment, the agent reactive with the cell surface marker is a ligand for the cell surface marker, such as a soluble ligand or a soluble ligand fusion protein (e.g., an Ig fusion protein). Soluble ligands can be prepared using standard recombinant DNA techniques, for example by deletion of the transmembrane and cytoplasmic domains. A soluble ligand can be transformed into a soluble ligand fusion protein also using standard recombinant DNA techniques. A fusion protein can be prepared in which fusion partner can comprise a binding moiety that facilitates separation of the fusion protein.

In order to separate the cell surface marker positive cells from non-reactive cells, one of a variety of different cell separation techniques known in the art can be used. Preferably, the cell surface marker positive cells are separated from non-reactive cells by fluorescence activated cell sorting (FACS). The FACS technology, and apparatuses for carrying it out to separate cells, is well established in the art. When FACS is used for cell separation, preferably the agent(s) reactive with the cell surface marker that is used is a fluorescently-labeled monoclonal antibody. Alternatively, cell separation can be achieved by, for example, magnetic activated cell sorting (MACS). When MACS is used for cell separation, preferably the agent reactive with the cell surface marker that is used is magnetic nanoparticles coated with monoclonal antibody. Alternatively, other single cell sorting methodologies known in the art can be applied to the methods of isolating human ventricular progenitor cells of the invention, including but not limited to IsoRaft array and DEPArray technologies.

Clonal Populations of Human Cardiac Ventricular Progenitor Cells

Clonal populations of HVPs can be obtained by expansion and propagation of the HVPs such that a clonal population of a billion or more cells can be achieved. The ability to clonally expand the human ventricular progenitor cells to such large numbers is a necessary feature for successful use of these cells in vivo to enhance cardiac function, since such a use requires on the order of a billion or more cells. As described further in the Examples, such a single cell can be obtained at approximately day 6 of the culture under conditions that promote the generation of cardiomyogenic progenitors. The clonal population of human cardiac ventricular progenitors can be further cultured and differentiated in vitro such that the cells express the ventricular maker MLC2v. Preferably, the single human cardiac ventricular progenitor cell is isolated by fluorescence activated cell sorting. Alternatively, the cell can be isolated by MACS or by other cell sorting methods known in the art and/or described herein. Preferably, the single human cardiac ventricular progenitor cell is cultured in Cardiac Progenitor Culture (CPC) medium, as described herein (see e.g., Example 3).

Pharmaceutical compositions comprising the clonal population of cardiac ventricular progenitor cells can be prepared by standard methods known in the art. The pharmaceutical compositions typically are sterile and can comprise buffers, media, excipients and the like suitable for pharmaceutical administration. In one embodiment, the pharmaceutical composition comprising the clonal population is formulated onto a three dimensional (3D) matrix. Compositions formulated onto a 3D matrix are particularly preferred for formation of a heart muscle cell patch that can be transplanted in vivo for heart muscle repair. Furthermore, the compositions can be formulated into two dimensional (2D) sheets of cells, such as a muscular thin film (MTF) as described in Domian, I. J. et al. (2009) Science 326:426-429. Such 2D sheets of cell tissue also can be used in the formation of a heart muscle cell patch that can be transplanted in vivo for heart muscle repair.

In Vivo Tissue Engineering

In vivo transplantation studies, described in Example 7 and 8 in which the human ventricular progenitors (HVPs) were transplanted under the kidney capsule in nude mice, document the ability of the HVPs to spontaneously assemble into a large wall of mature, functional, human ventricular muscle on the surface of the kidney capsule. Vascularization occurs via a paracrine pathway by calling the murine vasculature to the ventricular muscle wall, while a matrix is generated via a cell autonomous pathway from the progenitors themselves. In vivo intra-myocardial transplantation studies described in Example 9 in which the HVPs were transplanted into the normal murine heart document that the HVPs spontaneously migrate to the epicardial surface, where they expand, subsequently differentiate, and mature into a wall of human ventricular muscle on the surface of the epicardium. Taken together, these studies show that human ventriculogenesis can occur via a completely cell autonomous pathway in vivo via purified HVPs, thereby allowing their use in organ-on-organ in vivo tissue engineering.

The human ventricular myocardium has a limited capacity for regeneration, most of which is lost after 10 years of age (Bergmann, O. et al. (2015) Cell 161:1566-1575). As such, new strategies to generate heart muscle repair, regeneration, and tissue engineering approaches during cardiac injury have been a subject of intense investigation in regenerative biology and medicine (Sahara, M. et al. (2015) EMBO J. 34:710-738; Segers, V. F. M. and Lee, R. T. (2008) Nature 451:937-942). Given the need to achieve coordinated vascularization and matrix formation during tissue engineering of any solid organ, the assumption has been that the formation of an intact 3-D solid organ in vivo will ultimately require the addition of vascular cells and/or conduits, as well as biomaterials and/or decellularized matrix that will allow alignment and the generation of contractile force (Forbes, S. J. and Rosenthal, N. (2014) Nature Med. 20:857-869; Harrison, R. H. et al. (2014) Tissue Eng. Part B Rev. 20:1-16). The complexity of adding these various components to achieve the formation of a functional solid organ has confounded attempts to reduce this to clinical practice (Webber, M. J. et al. (2014) Ann. Biomed. Eng. 43:641-656). Although hPSCs hold great promise, to date, it has not been possible to build a pure, vascularized, fully functional, and mature 3-D human ventricular muscle organ in vivo on the surface of a heart in any mammalian system (Vunjak-Novakovic, G. et al. (2011) Annu. Rev. Biomed. Eng. 13:245-267).

The ability of generate billions of purified HVPs from a renewable source of either human ES or iPS cell lines, and detect engraftment markers indicative of the ability of the cells to engraft in vivo, represents a new approach to the generation of functional ventricular muscle in the setting of advanced heart failure. The progenitors can be delivered by intramyocardial injection and then self-migrate to the epicardial surface where they expand and differentiate, losing progenitor markers. Over the course of several week, the cells exit the cell cycle, and proceed to form adult rod-shaped cells that display several independent markers of mature ventricular myocardium including the formation of T tubules, catecholamine responsiveness, loss of automaticity, adult rod shaped conformation with aligned sarcomeric structures, and the ability to generate force that is comparable to other heart muscle patches derived from hPSCs differentiated cardiomyocytes (Tulloch, N. L. et al. (2011) Circ. Res. 109:47-59). The scalability of this cell autonomous pathway has allowed the ectopic generation of human ventricular muscle that has a combined thickness in excess of 1.5 cm in thickness, approaching levels that correspond to the human ventricular free wall (Basavarajaiah, S. et al. (2007) Br. J. Sports Med. 41:784-788).

The ability to migrate to the epicardial niche, the site of most of the adult heart progenitors at later stages, is a unique feature of HVPs, and mimics the normal niche of these cells during expansion of the ventricular compact zone during ventriculogenesis. Previous studies have shown that the generation of acute ischemic injury and a breakdown in vascular permeability are a pre-requisite for the grafting of relatively small numbers of ES cell derived cardiomyocytes into injured myocardium (van Laake, L. W. et al. (2007) Stem Cell Res. 1:9-24; Laflamme, M. A. et al. (2007) Nat. Biotechnol. 25:1015-1024), and even then the survival rate is low (<5%) (Laflamme, M. A. and Murry, C. E. (2011) Nature 473:326-335; Laflamme, M. A. et al. (2005) Am. J. Pathol. 167:663-671). The ability of intra-myocardial HVPs to form an extensive ventricular patch on the epicardial surface in the absence of acute ischemic injury provides a new therapeutic strategy for dilated cardiomyopathy without the need for additional biomaterials, cells, or transfer of exogenous genes and/or RNAs.

The ability to form a 3-D ventricular muscle wall on the epicardial surface of the in vivo normal heart is a unique feature of the ISL1/FZD4/JAG1/LIFR/FGFR3/TNFSF9 ventricular progenitors as later stage progenitors do not display the ability for the formation of three-dimensional ventricular tissue in either the cardiac or non-cardiac context, emphasizing the importance of generating a committed ventricular lineage as well as purifying the specific ventricular progenitor at a specific stage of ventriculogenesis.

Accordingly, the invention provides methods for generating human ventricular tissue in vivo using the HVPs described herein. In one embodiment, the method comprises transplanting engraftable HVPs into an organ of a non-human animal wherein the engraftable HVPs (i) express at least one cell surface marker selected from the group consisting of JAG1, FZD4, LIFR, FGFR3 and TNFSF9; and (ii) express at least one engraftment marker; and allowing the HVPs to grow in vivo such that human ventricular tissue is generated. Preferably, the non-human animal is immunodeficient such that it cannot mount an immune response against the human progenitor cells. In one embodiment, the non-human animal is a mouse, such as an immunodeficient NOD.Cg-Prkdcscid Il2rgtm1Wjl/SzJ mouse or an immunodeficient SCID-beige mouse (commercially available from Charles River France). In one embodiment, the organ is a kidney (e.g., the cells are transplanted under the kidney capsule). In another embodiment, the organ is a heart. In various embodiments, at least 1×10⁶ cells, at least 2×10⁶ cells, at least 3×10⁶ cells, at least 4×10⁶ cells, at least 5×10⁶ cells, at least 1×10⁷ cells, at least 5×10⁷ cells, at least 1×10⁸ cells, at least 1×10⁹ cells are transplanted.

To obtain engraftable HVPs for transplantation, human pluripotent stem cells (hPSCs) can be cultured in vitro under conditions leading to the generation of HVPs, as described herein (referred to herein as the HVPG protocol), followed by detection of the requisite cell surface marker(s) and engraftment marker(s).

Regarding the timing of transplanting HVPs post in-vitro culture, for optimal ventricular tissue generation the cells should be transplanted at a stage that can be defined based on the cellular markers expressed by the HVPs at the time of transplantation, determined at days post the start of culture, which is defined as day 0 of the HVPG protocol. In one embodiment, the cells are transplanted after the peak of cardiac mesoderm formation, which can be defined as peak expression of the mesodermal marker MESP1. Typically, MESP1 expression is between day 2 and day 4 of culture (inclusive) and peaks at day 3. In one embodiment, the cells are transplanted at the time corresponding to peak Islet-1 expression. Typically, Islet 1 is expressed between day 4 to day 8 of culture (inclusive) and peaks at day 6 of culture. In one embodiment, the cells are transplanted before the peak of NKX2.5 expression. Typically, NKX2.5 expression starts at day 6 of culture, peaks at day 10 of culture and is then maintained afterwards. In one embodiment, the cells are transplanted prior to the peak expression of the downstream genes MEF-2 and TBX-1. Typically, these downstream genes are expressed between day 5 and day 15 of culture (inclusive) and peaks at day 8 of culture. In one embodiment, the cells are transplanted prior to the expression of differentiated contractile protein genes. Typically, the expression of contractile protein genes (including TNNT2 and MYH6) starts from day 10 of culture onward. In certain embodiments, the cells are transplanted at a time when two, three or four of the aforementioned marker patterns are present. In another embodiment, the cells are transplanted at a time when all five of the aforementioned marker patterns are present. In one embodiment, the cells are transplanted between day 4 to day 8 (inclusive) of culture. In a more preferred embodiment, the cells are transplanted between day 5 to day 7 (inclusive) of culture. In the most preferred embodiment, the cells are transplanted on day 6 of culture.

The transplanted cells can be allowed to grow in the non-human animal for a suitable period time to allow for the generation of the desired size, amount or thickness of ventricular tissue. In various embodiments, the cells are allowed to grow for one week, two weeks, one month, two months, three months, four months, five months or six months. The method can further comprise harvesting ventricular tissue from the non-human animal after growth of the cells and differentiation into ventricular tissue.

Methods of Enhancing Cardiac Function

The methods of the invention for identifying and engrafting engraftable HVPs can be used in vivo to enhance cardiac function by transplanting the cells directly into the heart. It has now been shown that the HVPs have the capacity to differentiate into all three types of cardiac lineage cells (cardiac myocytes, endothelial cells and smooth muscle cells) (see Example 3). Furthermore, when cultured under conditions that bias toward the ventricular lineage, the HVPs have been shown to adopt a predominantly ventricular muscle phenotype when transplanted into the natural ventricle environment in vivo, demonstrating that these progenitor cells “recognize” the ventricular environment and respond and differentiate appropriately in vivo. Since damage to the ventricular environment is largely responsible for the impaired cardiac function in cardiac diseases and disorders, the ability to restore ventricular muscle cells using the ventricular progenitor cells of the invention represents a significant advance in the art.

To enhance cardiac function, preferably a clonal population of HVPs (e.g., in a pharmaceutical composition) is administered directly into the heart of the subject. More preferably, the clonal population is administered directly into a ventricular region of the heart of the subject. In one embodiment, the pharmaceutical composition administered to the subject comprises the clonal population formulated onto a three dimensional matrix.

The methods of the invention for enhancing cardiac function in a subject can be used in a variety of clinical situations involving damage to the heart or reduced or impaired cardiac function, such as in cardiovascular conditions, diseases and disorders. Non-limiting examples of such clinical situations include a subject who has suffered a myocardial infarction and a subject who has a congenital heart disorder. Examples of preferred cardiovascular conditions, diseases or disorders include coronary artery disease and acute coronary syndrome.

Methods of Use of Cardiac Ventricular Progenitor Cells In Vitro

The cardiac ventricular progenitor cells of the invention identified as expressing at least one cell surface marker (JAG1, FZD4, LIFR, FGFR3 and/or TNFSF9), as well as at least one engraftment marker (angiogenic markers and/or extracellular matrix markers) can be used in vitro in the study of various aspects of cardiac maturation and differentiation, in particular in identifying the cells signaling pathways and biological mediators involved in the process of cardiac maturation and differentiation.

Furthermore, since cardiac ventricular progenitor cells are committed to the cardiac lineage and, moreover, are biased toward ventricular differentiation, these progenitor cells also are useful for evaluating the cardiac toxicity of test compounds. All potential new drugs and therapeutics must be evaluated for their toxicity to cardiac cells, before they can be deemed safe for use in humans. Thus, the ability to assess cardiac toxicity in an in vitro culture system is very advantageous. Accordingly, in another aspect, the invention provides a method of screening for cardiac toxicity of test compound, the method comprising

Providing human cardiac ventricular progenitor cells that (i) express at least one cell surface marker selected from the group consisting of JAG1, FZD4, LIFR, FGFR3 and TNFSF9; and (ii) express at least one engraftment marker;

contacting the cells with the test compound; and

measuring toxicity of the test compound for the cells,

wherein toxicity of the test compound for the cells indicates cardiac toxicity of the test compound.

In a preferred embodiment, the HVPs are provided by isolating the cells according to the methods described herein. In a particularly preferred embodiment, the cells are isolated by separating cell surface marker expressing cells from a cell culture comprising cardiac progenitor cells using an antibody that specifically binds to the cell surface marker. Preferably, the cells are isolated using FACS or MACS as described herein. In yet another embodiment, the HVPs are further cultured and differentiation into MLC2v+ ventricular cells prior to contacting with the test compound.

The toxicity of the test compound for the cells can be measured by one or more of a variety of different methods for assessing cell viability or other physiological functions. Preferably, the effect of the test compound on cell viability is measured using a standard cell viability assay, wherein reduced cell viability in the presence of the test compound is indicative of cardiac toxicity of the test compound. Additionally or alternatively, cell growth can be measured. Additionally or alternatively, other indicators of physiological functions can be measured, such as cell adhesion, cell signaling, surface marker expression, gene expression and the like. Similarly, a negative effect of the test compound on any of these indicators of physiological function is indicative of cardiac toxicity of the test compound.

The invention further provides a method of identifying a compound that modulates human cardiac ventricular progenitor cell differentiation, the method comprising

providing human cardiac ventricular progenitor cells that (i) express at least one cell surface marker selected from the group consisting of JAG1, FZD4, LIFR, FGFR3 and TNFSF9; and (ii) express at least one engraftment marker;

culturing the cells in the presence or absence of a test compound;

measuring differentiation of the cells in the presence or absence of the test compound; and

selecting a test compound that modulates human cardiac ventricular progenitor cell differentiation, as compared to differentiation in the absence of the test compound, to thereby identify a compound that modulates human cardiac ventricular progenitor cell differentiation.

In one embodiment, the test compound stimulates human cardiac ventricular progenitor cell differentiation. In another embodiment, the test compound inhibits human cardiac ventricular progenitor cell differentiation. Differentiation of the cells can be measured by, for example, measurement of the expression of differentiation markers appearing on the cultured cells over time, as described herein. In a preferred embodiment, the HVPs are provided by isolating the cells according to the methods described herein. In a particularly preferred embodiment, the cells are isolated by separating cell surface marker expressing cells from a cell culture comprising cardiac progenitor cells using an antibody that specifically binds to the cell surface marker. Preferably, the cells are isolated using FACS or MACS as described herein.

The invention further provides a method of identifying a compound that modulates human ventricular cardiomyocyte function, the method comprising

providing human cardiac ventricular progenitor cells that (i) express at least one cell surface marker selected from the group consisting of JAG1, FZD4, LIFR, FGFR3 and TNFSF9; and (ii) express at least one engraftment marker;

culturing the cells in the presence or absence of a test compound under conditions that generate human ventricular cardiomyocytes;

measuring function of the human ventricular cardiomyocytes in the presence or absence of the test compound; and

selecting a test compound that modulates human ventricular cardiomyocyte function, as compared to function in the absence of the test compound, to thereby identify a compound that modulates human ventricular cardiomyocyte function.

In one embodiment, the test compound stimulates human ventricular cardiomyocyte function. In another embodiment, the test compound inhibits human ventricular cardiomyocyte function. Function of the cells can be measured by measurement of any suitable indicator of ventricular cell function, including but not limited to, for example, formation of T tubules, acquisition of adult-rod shaped ventricular cardiomyocytes, and ability to generate force in response to electrical stimulation. Suitable assays for measuring such indicators of ventricular cell function are known in the art. In a preferred embodiment, the HVPs are provided by isolating the cells according to the methods described herein. In a particularly preferred embodiment, the cells are isolated by separating cell surface marker expressing cells from a cell culture comprising cardiac progenitor cells using an antibody that specifically binds to the cell surface marker. Preferably, the cells are isolated using FACS or MACS as described herein.

In Vivo Animal Models Using Human Ventricular Progenitor Cells

The development of human iPS and ES cell based models of cardiac disease has opened new horizons in cardiovascular drug development and discovery. However, to date, these systems have had the limitations of being based on 2D structures in cultured cell systems. In addition, the fetal and immature properties of the cells limit their utility and fidelity to the adult heart. Human cardiac disease, in particular heart failure, is a complex, multifactoral, multi-organ disease, that is influenced by environmental, hormonal, and other key organs that are known sites for therapeutic targets, such as the kidney. The ability to build a mature functional human ventricular organ either ectopically or on the surface of the intact normal murine heart opens up a new in vivo model system to allow studies that normally could only be assayed on a mature human ventricular muscle chamber, such as ventricular arrhythmias, generation of contractile force, fibrosis, and the potential for regeneration. Accordingly, the option to study human cardiac disease outside of the in vitro tissue culture systems, and directly in the context of heart failure in vivo, is now clearly possible.

Thus, the engraftable HVPs identified according to the methods of the invention also can be used to create animal models that allow for in vivo assessment of human cardiac tissue function and for in vivo screening of compounds, such as to determine the cardiac toxicity of a test compound in vivo or to identify compounds that modulate human cardiac tissue differentiation or function in vivo. Accordingly, the invention provides methods for testing the effects of test compounds on human ventricular tissue in vivo using the HVPs described herein. In one embodiment, the method comprises:

transplanting engraftable HVPs into an organ of a non-human animal wherein the engraftable HVPs (i) express at least one cell surface marker selected from the group consisting of JAG1, FZD4, LIFR, FGFR3 and TNFSF9; and (ii) express at least one engraftment marker;

allowing the progenitors to grow in vivo such that human ventricular tissue is generated;

administering a test compound to the non-human animal; and

evaluating the effect of the test compound on the human ventricular tissue in the non-human animal.

In another embodiment, the method comprises:

administering a test compound to a non-human animal, wherein the non-human animal comprises engraftable human ventricular progenitors (HVPs) transplanted into an organ of the non-human animal, wherein the engraftable HVPs (i) express at least one cell surface marker selected from the group consisting of JAG1, FZD4, LIFR, FGFR3 and TNFSF9; and (ii) express at least one engraftment marker; and

evaluating the effect of the test compound on the engraftable HVPs in the non-human animal.

In one embodiment, the cardiac toxicity of the test compound is evaluated, for example by measuring the effect of the test compound on the viability of the human ventricular tissue or the human ventricular progenitors in the non-human animal (as compared to the viability of the tissue or progenitors in the absence of the test compound). Cell viability can be assessed by standard methods known in the art.

In another embodiment, the ability of a test compound to modulate cardiac differentiation can be evaluated, for example by measuring the effect of the test compound on the differentiation of the human ventricular tissue or HVPs in the non-human animal (as compared to the differentiation of the tissue or progenitors in the absence of the test compound). Differentiation of the cells can be measured by, for example, measurement of the expression of differentiation markers appearing on the cells over time.

In another embodiment, the ability of a test compound to modulate cardiac function can be evaluated, for example by measuring the effect of the test compound on the function of the human ventricular tissue or HVPs in the non-human animal (as compared to the function of the tissue or HVPs in the absence of the test compound). Function of the tissue or HVPs can be measured by measurement of any suitable indicator of ventricular cell function, including but not limited to, for example, formation of T tubules, acquisition of adult-rod shaped ventricular cardiomyocytes, and ability to generate force in response to electrical stimulation. Suitable assays for measuring such indicators of ventricular cell function are known in the art.

Preferably, the non-human animal is immunodeficient such that it cannot mount an immune response against the human progenitor cells. In one embodiment, the non-human animal is a mouse, such as an immunodeficient NOD.Cg-Prkdcscid Il2rgtm1Wjl/SzJ mouse or an immunodeficient SCID-beige mouse (commercially available from Charles River France). In one embodiment, the organ is a kidney (e.g., the cells are transplanted under the kidney capsule). In another embodiment, the organ is a heart. In various embodiments, at least 1×10⁶ cells, at least 2×10⁶ cells, at least 3×10⁶ cells, at least 4×10⁶ cells, at least 5×10⁶ cells, at least 1×10⁷ cells, at least 5×10⁷ cells, at least 1×10⁸ cells, at least 1×10⁹ cells are transplanted.

To create the animal models, engraftable HVPs for transplantation can be obtained as described above by culturing of hPSCs in vitro under conditions leading to the generation of HVPs, followed by detection of the requisite cell surface marker(s) and engraftment marker(s). Regarding the timing of transplanting HVPs post in-vitro culture, for optimal ventricular tissue generation the cells should be transplanted at a stage that can be defined based on the cellular markers expressed by the HVPs at the time of transplantation, determined at days post the start of culture, which is defined as day 0 of the HVPG protocol. In one embodiment, the cells are transplanted after the peak of cardiac mesoderm formation, which can be defined as peak expression of the mesodermal marker MESP1. Typically, MESP1 expression is between day 2 and day 4 of culture (inclusive) and peaks at day 3. In one embodiment, the cells are transplanted at the time corresponding to peak Islet-1 expression. Typically, Islet 1 is expressed between day 4 to day 8 of culture (inclusive) and peaks at day 6 of culture. In one embodiment, the cells are transplanted before the peak of NKX2.5 expression. Typically, NKX2.5 expression starts at day 6 of culture, peaks at day 10 of culture and is then maintained afterwards. In one embodiment, the cells are transplanted prior to the peak expression of the downstream genes MEF-2 and TBX-1. Typically, these downstream genes are expressed between day 5 and day 15 of culture (inclusive) and peaks at day 8 of culture. In one embodiment, the cells are transplanted prior to the expression of differentiated contractile protein genes. Typically, the expression of contractile protein genes (including TNNT2 and MYH6) starts from day 10 of culture onward. In certain embodiments, the cells are transplanted at a time when two, three or four of the aforementioned marker patterns are present. In another embodiment, the cells are transplanted at a time when all five of the aforementioned marker patterns are present. In one embodiment, the cells are transplanted between day 4 to day 8 (inclusive) of culture. In a more preferred embodiment, the cells are transplanted between day 5 to day 7 (inclusive) of culture. In the most preferred embodiment, the cells are transplanted on day 6 of culture.

The transplanted cells can be allowed to grow in the non-human animal for a suitable period time to allow for the generation of the desired size, amount or thickness of ventricular tissue, prior to administration of the test compound(s). In various embodiments, the cells are allowed to grow for one week, two weeks. one month, two months, three months, four months, five months or six months.

Kits

In another aspect, the invention provides kits for preparing engraftable HVPs. In one embodiment, the kit comprises means for isolating HVPs expressing at least one cell surface marker selected from the group consisting of JAG1, FZD4, LIFR, FGFR3 and TNFSF9 and means for detecting at least one engraftment marker expressed by the isolated HVPs, along with instructions for use of the kit to isolate engraftable HVPs. In one embodiment, the kit comprises means for detecting at least one angiogenic engraftment marker (positive and/or negative angiogenic marker(s)). In another embodiment, the kit comprises means for detecting at least one extracellular matrix engraftment marker (positive and/or negative extracellular matrix marker(s)). In yet another embodiment, the kit comprises means for detecting at least one angiogenic engraftment marker and at least one extracellular matrix engraftment marker. Means for detecting any of the engraftment markers described above with respect to the methods of identifying and transplanting engraftable HVPs can be included in a kit of the invention. Preferred angiogenic markers for detection in a kit of the invention include FGF10, PRKD1, CCBE1, PDGFRA, EPHB2, GATA2 and NTRK1. Preferred extracellular matrix markers for detection in a kit of the invention include FGF10, SMOC1 and CCBE1.

In one embodiment, the means for isolating the HVPS expressing at least one cell surface marker selected from the group consisting of JAG1, FZD4, LIFR, FGFR3 and TNFSF9 is one or more agents reactive with the one or more of the cell surface marker(s). In one embodiment, the agent(s) reactive with the cell surface marker(s) is an antibody that specifically binds to the cell surface marker, such as a monoclonal antibody. Non-limiting examples of such agents include murine, rabbit, human, humanized or chimeric monoclonal antibodies with binding specificity for the cells surface marker (e.g., anti-JAG1, anti-FZD4, anti-LIFR, anti-FGFR3 and/or anti-TNFSF9 antibodies). Such monoclonal antibodies are commercially available in the art (e.g., R&D Systems, Santa Cruz Biotechnology). Moreover, such antibodies can be prepared using standard techniques well established in the art using the cell surface marker as the antigen. In another embodiment, the agent reactive with the cell surface marker is a ligand for the cell surface marker, such as a soluble ligand or a soluble ligand fusion protein (e.g., an Ig fusion protein). Soluble ligands can be prepared using standard recombinant DNA techniques, for example by deletion of the transmembrane and cytoplasmic domains. A soluble ligand can be transformed into a soluble ligand fusion protein also using standard recombinant DNA techniques. A fusion protein can be prepared in which fusion partner can comprise a binding moiety that facilitates separation of the fusion protein.

In one embodiment, the means for detecting the at least one engraftment marker is one or more nucleic acids that detect RNA (e.g., mRNA) or DNA (e.g., cDNA) encoding the engraftment marker(s). In one embodiment, the nucleic acid(s) that detects RNA or DNA encoding the engraftment marker(s) is an oligonucleotide probe capable of hybridizing to RNA or DNA encoding the engraftment marker(s). In another embodiment, the nucleic acid(s) that detects RNA or DNA encoding the engraftment marker(s) is a pair of oligonucleotide primers capable of amplifying nucleic acid encoding the engraftment marker(s), for example PCR primers. Such oligonucleotide probes and primers can be designed and prepared (e.g., synthesized) based on the publicly available nucleotide sequences of the engraftment markers disclosed herein using standard recombinant DNA methodologies.

In another embodiment, the means for detecting the at least one engraftment marker is one or more agents reactive with the engraftment marker protein. The agent(s) reactive with the engraftment marker protein(s) can be, for example, an antibody (e.g., monoclonal antibody or other suitable antibody as described above with respect to the agents reactive with the cell surface markers) or a ligand (e.g., soluble ligand or soluble ligand fusion protein, as described above with respect to the agents reactive with the cell surface markers). Suitable antibodies or ligand agents reactive with an engraftment marker protein are known in the art and/or can be prepared using standard recombinant DNA techniques.

The present invention is further illustrated by the following examples, which should not be construed as further limiting. The contents of FIGURES and all references, patents and published patent applications cited throughout this application are expressly incorporated herein by reference.

EXAMPLES Example 1: Generation of Human Isl1+ Cardiomyogenic Progenitor Cells by Modulation of Wnt Signaling in Human Pluripotent Stem Cells

Temporal modulation of canonical Wnt signaling has been shown to be sufficient to generate functional cardiomyocytes at high yield and purity from numerous hPSC lines (Lian, X. et al. (2012) Proc. Natl. Acad. Sci. USA 109:E1848-1857; Lian, X. et al. (2013) Nat. Protoc. 8:162-175). In this approach, Wnt/β-catenin signaling first is activated in the hPSCs, followed by an incubation period, followed by inhibition of Wnt/β-catenin signaling. In the originally published protocol, Wnt/β-catenin signaling activation was achieved by incubation with the Gsk3 inhibitor CHIR99021 (GSK-3 α, IC₅₀=10 nM; GSK-3, β IC₅₀=6.7 nM) and Wnt/β-catenin signaling inhibition was achieved by incubation with the Porcn inhibitor IWP2 (IC₅₀=27 nM). Because we used Gsk3 inhibitor and Wnt production inhibitor for cardiac differentiation, this protocol was termed GiWi protocol. To improve the efficiency of the original protocol and reduce the potential side effects of the small molecules used in the original protocol, a second generation protocol was developed that uses another set of small molecules with higher inhibition potency. In this second generation GiWi protocol, Wnt/β-catenin signaling activation was achieved by incubation with the Gsk3 inhibitor CHIR98014 (CAS 556813-39-9; commercially available from, e.g., Selleckchem) (GSK-3 α, IC₅₀=0.65 nM; GSK-3, β IC₅₀=0.58 nM) and Wnt/β-catenin signaling inhibition was achieved by incubation with the Porcn inhibitor Wnt-059 (CAS 1243243-89-1; commercially available from, e.g., Selleckchem or Tocris) (IC₅₀=74 pM). The Gsk3 inhibitor CHIR98014 was used to promote cardiac mesodermal differentiation, whereas the Porcn inhibitor Wnt-059 was used to enhance ventricular progenitor differentiation from mesoderm cells.

For cardiomyocyte differentiation via the use of these small molecules, hPSCs were maintained on Matrigel (BD Biosciences) coated plates (Corning) in E8 medium (described in Chen, G. et al. (2011) Nature Methods, 8:424-429; commercially available; STEMCELL Technologies) or mTeSR1 medium (commercially available; STEMCELL Technologies). Suitable hPSCs include induced pluripotent stem cells (iPSCs) such as 19-11-1, 19-9-7 or 6-9-9 cells (Yu, J. et al. (2009) Science, 324:797-801) and human embryonic stem cells (hESCs), such as ES03 (WiCell Research Institute) and H9 cells (Thomson, J. A. et al. (1998) Science, 282:1145-1147).

hPSCs maintained on a Matrigel-coated surface in mTeSR1 medium were dissociated into single cells with Accutase (Life Technologies) at 37° C. for 5 minutes and then seeded onto a Matrigel-coated cell culture dish at 100,000-200,000 cells/cm² in mTeSR1 medium supplemented with 5 μM ROCK inhibitor Y-27632 (Selleckchem)(day −2) for 24 hours. Cells were then cultured in mTeSR1, changed daily. At day 0, cells were then treated with 1 μM Gsk3 inhibitor CHIR98014 (Selleckchem) for 24 hours (day 0 to day 1) in RPMI/B27-ins (500 ml RPMI with 10 ml B27 supplement without insulin). The medium was then changed to the corresponding medium containing 2 μM the Porcn inhibitor Wnt-059 (Selleckchem) at day 3, which was then removed during the medium change on day 5. Cells were maintained in RPMI/B27 (stock solution: 500 ml RMPI medium+10 ml B27 supplement) starting from day 7, with the medium changed every three days. This exemplary culturing protocol for generating cardiomyogenic progenitor cells is illustrated schematically in the drawing.

Flow cytometry and immunostaining were preformed to examine the expression of particular lineage markers. After 24 hour treatment with CHIR-98014, more than 99% of the hPSCs expressed the mesoderm marker Brachyury. Three days after treatment with CHIR-98014, more than 95% of differentiated cells expressed Mespl, which marks the cardiac mesoderm. The culture protocol not only allowed the cells to synchronously differentiate into the cardiac mesodermal lineage, but also reproducibly generated more than 90% of ventricular myocytes after 14 days of differentiation, as determined by cTnT flow cytometry and electrophysiology analysis.

To further assess cardiac differentiation of the hPSCs over time, Western blot analysis was performed on days 0-7 and d11 to examine the expression of Isl1 and Nkx2.5 (cardiomyogenic progenitor markers) and cTnI (a cardiac myocyte marker). Cells were lysed in M-PER Mammalian Protein Extraction Reagent (Pierce) in the presence of Halt Protease and Phosphatase Inhibitor Cocktail (Pierce). Proteins were separated by 10% Tris-Glycine SDS/PAGE (Invitrogen) under denaturing conditions and transferred to a nitrocellulose membrane. After blocking with 5% dried milk in TBST, the membrane was incubated with primary antibody overnight at 4° C. The membrane was then washed, incubated with an anti-mouse/rabbit peroxidase-conjugated secondary antibody at room temperature for 1 hour, and developed by SuperSignal chemiluminescence (Pierce). During cardiac differentiation of hPSCs, Isl1 expression started on day 4 and increased to its maximum expression on day 6, whereas NKx2.5 only started to express on day 6 and reached its maximum expression after day 10. Cardiomyoctes (cTnI+ cells) were not induced until day 11 of differentiation.

In addition, immunostaining of the day 6 cells was performed for Isl1 expression. Cells were fixed with 4% formaldehyde for 15 minutes at room temperature and then stained with primary (anti-Isl1) and secondary antibodies in PBS plus 0.4% Triton X-100 and 5% non-fat dry milk (Bio-Rad). Nuclei were stained with Gold Anti-fade Reagent with DAPI (Invitrogen). An epifluorescence microscope (Leica DM IRB) with a QImaging® Retiga 4000R camera was used for imaging analysis. The results showed substantial numbers of Isl1+ cells.

Flow cytometry analysis of day 6 cells for Isl1 expression also was performed. Cells were dissociated into single cells with Accutase for 10 minutes and then fixed with 1% paraformaldehyde for 20 minutes at room temperature and stained with primary and secondary antibodies in PBS 0.1% Triton X-100 and 0.5% BSA. Data were collected on a FACSCaliber flow cytometer (Beckton Dickinson) and analyzed using FloJo. The results showed that more than 95% of cells expressed Isl1 at this stage.

In summary, this example provides a protocol for human ventricular progenitor generation (HVPG protocol) that allows for the large-scale production of billions of Isl1+ human HPVs efficiently within 6 days.

Example 2: Identification of Jagged 1 as a Cell Surface Marker of Human Ventricular Progenitor Cells

To profile the transcriptional changes that occur during the cardiac differentiation process at a genome-scale level, RNA sequencing (RNA-seq) was performed at different time points following differentiation to build cardiac development transcriptional landscapes. We performed RNA-seq experiments on day 0 to day 7 samples, as well as day 19 and day 35 samples (two independent biological replicates per time point). Two batches of RNA-seq (100 bp and 50 bp read length) were performed using the illumine Hiseq 2000 platform. In total, 20 samples were examined. Bowtie and Tophat were used to map our reads into a reference human genome (hg19) and we calculate each gene expression (annotation of the genes according to Refseq) using RPKM method (Reads per kilobase transcript per million reads). Differentiation of hPSCs to cardiomyocytes involves five major cell types: pluripotent stem cells (day 0), mesoderm progenitors (day 1 to day 2), cardiac mesoderm cells (day 3 to day 4), heart field progenitors (day 5, day 6 and day 7), and cardiomyocytes (day 10 after).

Molecular mRNA analysis of cardiac differentiation from hPSCs using the HVPG protocol revealed dynamic changes in gene expression, with down-regulation of the pluripotency markers OCT4, NANOG and SOX2 during differentiation. Induction of the primitive streak-like genes T and MIXL1 occurred within the first 24 hours following CHIR-98014 addition, and was followed by upregulation of the cardiac mesodermal marker MESP1 on day 2 and day 3. Expression of the cardiac muscle markers TNNT2, TNNC1, MYL2, MYL7, MYH6, MYH7 and IRX4 was detected at later stage of differentiation (after day 10).

By this analysis, genes enriched at each differentiation stage, including mesoderm cells, cardiac progenitors and cardiomyocytes, were identified. Mesoderm cells, which are related to day 1 differentiated cells, express brachyury. We identified potential surface markers for mesoderm cells, including: FZD10, CD48, CD1D, CD8B, IL15RA, TNFRSF1B, TNFSF13, ICOSLG, SEMA7A, SLC3A2, SDC1, HLA-A. Through similar analysis, we also identified surface markers for cardiac mesoderm mespl positive cells, including: CXCR4, ANPEP, ITGA5, TNFRSF9, FZD2, CD1D, CD177, ACVRL1, ICAM1, L1CAM, NGFR, ABCG2, FZD7, TNFRSF13C, TNFRSF1B.

Consistent with western blot analysis, ISL1 mRNA was expressed as early as day 4 and peaked on day 5, one day before its protein expression reached its peak. On day 5 of differentiation (the cardiac progenitor stage, isl1 mRNA expression maximum on day 5, isl1 protein expression maximum on day 6), the day 5 enriched genes were compared with an anti-CD antibody array (a panel of 350 known CD antibodies) and a number of potential cell-surface protein markers were identified. We identified many cell-surface proteins expressed at this stage, including: FZD4, JAG1, PDGFRA, LIFR (CD118), TNFSF9, FGFR3.

The cell surface protein Jagged 1 (JAG1), Frizzled 4 (FZD4), LIFR (CD118) and FGFR3 were selected for further analysis. Jagged 1 expression was further studied as described below and in Example 3. Frizzled 4 expression was further studied as described in Example 4. LIFR (CD118) and FGFR3 expression was further studied as described in Example 5.

Firstly, the expression of Isl1 and Jag1 was profiled using the double staining flow cytometry technique. Flow cytometric analysis was carried out essentially as described in Example 1, using anti-Isl1 and anti-Jag1 antibodies for double staining. Jagged 1 expression was found to trace the expression of Islet 1 and on day 6 of differentiation, all of the Islet 1 positive cells also expressed Jagged 1, and vice versa. Because of the co-expression pattern of these two markers, a Jagged 1 antibody was used to enrich the 94.1% Islet 1+ cells differentiated population to 99.8% purity of Islet1+Jagged1+ cells.

It also was confirmed that Islet 1 is an earlier developmental gene than the Nkx2.5 gene using double immunostaining of ISL1 and NKX2.5 expression in HVPs. The purified HVPs uniformly express the ISL1 gene, but at this stage, only a few of the cells started to express Nkx2.5.

Furthermore, immunostaining with both anti-Isl1 and anti-Jag 1 was performed, essentially as described in Example 1, on week 4 human fetal heart tissue, neonatal heart tissue and 8-year old heart tissue. The results revealed that in the in vivo fetal heart, all of the Islet 1 positive cells also expressed Jagged 1. However, the neonatal heart and 8-year old heart did not express Islet 1 or Jagged 1. In the ventricle of week 4 human fetal heart, cardiac Troponin T (cTnT) staining revealed visible sarcomere structures. In addition, over 50% of ventricular cells in the week 4 fetal heart expressed both Islet1 and Jagged1, which was markedly decreased during subsequent maturation, with the loss of expression of both Islet1 and Jagged1 in the ventricular muscle cells of the human neonatal hearts.

The above-described experiments demonstrate that Jagged 1 is a cell surface marker for Islet 1 positive cardiomyogenic progenitor cells.

Example 3: Clonal Differentiation of Isl1+Jag1+ Cardiac Progenitor Cells

To characterize the clonal differentiation potential of Isl1+Jag1+ cells, cardiomyogenic progenitor cells were generated by the culturing protocol described in Example 1, and one single Isl1+Jag1+ cell was seeded into one well of a Matrigel-coated 48-well plate. Cells were purified with antibody of Jag1 and then one single cell was seeded into one well. The single cells were then cultured for 3 weeks in Cardiac Progenitor Culture (CPC) medium (advanced DMEM/F12 supplemented with 2.5 mM GlutaMAX, 100 μg/ml Vitamin C, 20% Knockout Serum Replacement).

Immunostaining of the 3-week differentiation cell population was then performed with three antibodies: cardiac troponin I (cTn1) for cardiomyocytes, CD144 (VE-cadherin) for endothelial cells and smooth muscle actin (SMA) for smooth muscle cells. The results showed that the single cell-cultured, Isl1+Jag1+ cells gave rise to cTnI positive and SMA positive cells, but not VE-cadherin positive endothelial cells, indicating these generated Islet1+ cells are heart muscle progenitors that have limited differentiation potential to endothelial lineages. Purified Islet1+Jagged1+ cells differentiated with the HVPG protocol from human induced pluripotent stem cells (iPSC 19-9-11 line) also showed similar in vitro differentiation potential and predominantly differentiate to cTnI+SMA+ cells, but not VE-cadherin+ cells. Over the course of several weeks, the cells expressed the ventricular specific marker MLC2v, indicating that the initial ISL1+ subset was already committed to the ventricular cell fate. Because of the limited vascular differentiation potential of Islet1+ cells generated using the HVPG protocol, these generated Islet1+ cells might represent a distinct progenitor population from the previously reported KDR+ population (Yang, L. et al. (2008) Nature 453:524-528) or multipotent ISL1+ cells (Bu, L. et al. (2009) Nature 460:113-117; Moretti, A. et al. (2006) Cell 127:1151-1165), which can give rise to all three lineages of cardiovascular cells.

These results demonstrated that the Isl1+Jag1+ cardiomyogenic progenitor cells can be successfully cultured in vitro from a single cell to a significantly expanded cell population (1×10⁹ cells or greater) that contains all three types of cardiac lineage cells, with a predominance of cardiomyocytes. Furthermore, these cells can be cultured in vitro for extended periods of time, for at least 2-3 weeks, and even for months (e.g., six months or more). Since the cardiomyogenic progenitor cells gradually differentiate into cardiomyocytes, which do not proliferate, a culture period of approximately 2-3 weeks is preferred.

Example 4: Identification of Frizzled 4 as a Cell Surface Marker of Cardiac Progenitor Cells

As described in Example 2, Frizzled 4 (FZD4) was identified by RNA-seq analysis as being expressed in cardiac progenitor cells. Thus, to confirm FZD4 as a cell surface marker of cardiac progenitor cells, FZD4 expression was assessed during cardiac differentiation via Western blot analysis. The results demonstrated that FZD4 was not expressed in pluripotent stem cells and the first 3 days differentiated cells. However, FZD4 started to express on day 4 and maximize its expression on day 5 of expression.

In order to quantify the co-expression pattern of FZD4 and Isl1 at the single cell level, FACS analysis was performed. On day 5 of differentiation, more than 83% of cells express both isl1 and FZD4, demonstrating that FZD4 is a cell surface marker for Isl1 positive cells during cardiac progenitor differentiation using the GiWi protocol.

In order to confirm that both JAG1 and FZD4 were indeed co-expressed with ISL1 on the human ventricular progenitor cells, triple immunofluorescence analysis of day 6 differentiated cells from hPSCs was performed with antibodies to Islet 1, Jagged 1 and Frizzled 4. The triple staining experiment demonstrated that Isl1+ cells expressed both Jagged 1 and Frizzled 4.

Example 5: Identification of Leukemia Inhibitor Factor Receptor (LIFR) and Fibroblast Growth Factor Receptor 3 (FGFR3) as Cell Surface Markers of Cardiac Progenitor Cells

As described in Example 2, LIFR(CD118) and FGFR3 were identified by RNA-seq analysis as being expressed in cardiac progenitor cells. In this example, expression of these additional cell surface markers for the human ventricular progenitor cells was confirmed by flow cytometry analysis. Human ventricular progenitor (HVP) cells were generated as described in Example 1 or 11 and day 6 cells were analyzed by standard flow cytometry. A double staining flow cytometry experiment using anti-Islet 1 and anti-Leukemia Inhibitory Factor Receptor (LIFR) antibodies was performed. The results demonstrate that the HVP cells co-express Islet 1 and LIFR, thereby confirming that LIFR is a cell surface marker for the HVP cells. Furthermore, flow cytometry experiments were performed comparing the expression of LIFR and Fibroblast Growth Factor Receptor 3 (FGFR3) on day 6 HVP cells to undifferentiated embryonic stem (ES) cells. The results demonstrate that LIFR and FGFR3 are both highly enriched for expression on the HVP cells, thereby confirming that LIFR and FGFR3 are both cell surface markers for the HVP cells.

Example 6: In Vivo Developmental Potential of Isl1+Jag1+ Cardiac Progenitor Cells'

The ES03 human embryonic stem cell (hESC) line (obtained from WiCell Research Institute) expresses green fluorescent protein (GFP) driven by the cardiac-specific cTnT promoter. ES03 cells were used to generate Isl1+Jag1+ cardiomyogenic progenitor cells using the culturing protocol described in Example 1. The Isl1+Jag1+ cardiomyogenic progenitor cells were transplanted into the hearts of severe combined immunodeficient (SCID) beige mice to document their developmental potential in vivo.

Briefly, Isl1+Jag1+ cells were injected (1,000,000 cells per recipient) directly into the left ventricular wall of NOD/SCID-gamma mice in an open-chest procedure. Hearts were harvested 2-3 weeks post surgery, fixed in 1% PFA and sectioned at 10 μm (n=12). Histological analyses of the hearts of the transplanted mice revealed the presence of GFP+ donor cells, detected by epifluorescence and by staining with an anti-GFP antibody, demonstrating that the Isl1+Jag1+ cardiomyogenic progenitor cells were capable of differentiating into cardiomyocytes when transplanted in vivo.

The Isl1+Jag1+ cardiomyogenic progenitor cells were also transplanted directly into infarcted hearts of SCID beige mice (“injured mice”), as compared to similarly transplanted normal mice. When analyzed two weeks later, injured mice transplanted with the Isl1+Jag1+ cardiomyogenic progenitor cells had a larger graft size than the normal mice similarly transplanted, demonstrating the cardiomyocyte regeneration capacity of the Isl1+Jag1+ cardiomyogenic progenitor cells in vivo.

Example 7: Human Ventricular Progenitors (HPVs) Generate a 3-D Ventricular Heart Muscle Organ In Vivo

The building of the ventricular heart muscle chamber is one of the most critical and earliest steps during human organogenesis, and requires a series of coordinated steps, including migration, proliferation, vascularization, assembly, and matrix alignment. To test the capacity of HVPs to drive ventriculogenesis in vivo, we transplanted purified HVPs or unpurified HVPs (92.0±1.9% ISL1+) under the kidney capsule of immunocompromised mice. After 2 months post-transplantation, animals transplanted with unpurified HVPs formed tumors, resulting in a tumor formation efficiency of 100% (100%, 4/4), whereas animals transplanted with purified HVPs did not form any tumors (0%, 0/10).

The engrafted kidneys with purified HVPs were further assayed for histological analysis. Hematoxylin and Eosin (H&E) staining revealed an organ that exceeded 0.5 cm in length with more than 1 mm thickness on the surface of the mouse kidney, and that uniformly expressed the ventricular specific marker MLC2v (O'Brien, T. X. et al. (1993) Proc. Natl. Acad. Sci. USA 90:5157-5161). The resulting human muscle organ was fully vascularized and red blood cells could be detected in the blood vessels. Analysis of cTnT, MLC2v, and MLC2a immunostaining further revealed that the transplanted HVPs not only differentiated into cardiac muscle cells (cTnT+ cells), but also further mature to become MLC2v+ ventricular myocytes that are negative for MLC2a expression. The resulting ventricular muscle organ is fully vascularized by murine derived vascular cells, consistent with the notion that its vascularization occurred via paracrine cues derived from the HVPs.

The blood vessel structured was revealed by immunostaining analysis of antibodies directed against VE-cadherin and smooth muscle actin expression. In addition, using a human specific monoclonal laminin antibody targeting laminin γ-1 chain, the HVPs secreted their own human laminin as their extracellular matrix (the mouse kidney region is negative for human laminin immunostaining). In addition, we found human fibronectin expression is restricted to areas near the blood vessels using a monoclonal human fibronectin antibody.

To assess the capacity of late stage cardiac cells to drive ventriculogenesis, NKX2.5+ cells (day 10 after differentiation) were transplanted under the kidney capsule of immunocompromised NSG mice. At three weeks post-transplantation, animals transplanted with NKX2.5+ cells did not form any visible human muscle graft, indicating that HVPs lose their ability for in vivo ventriculogenesis following peak Islet-1 expression.

Taken together, these studies indicate that the HVPs can synthesize and release their own cardiac laminin-derived matrix, as well as fibronectin which serves to stabilize the vasculature to the nascent ventricular organ.

Example 8: HVPs Create a Mature, Functioning Ventricular Muscle Organ In Vivo Via a Cell Autonomous Pathway

One of the critical limitations for the utility of hPSCs for studies of human cardiac biology and disease is their lack of maturity and persistence of expression of fetal isoforms. To determine if the HVP derived organs could become functional mature ventricular muscle, long term transplantation studies were performed followed by detailed analyses of a panel of well accepted features of adult ventricular myocardium including formation of T tubules (Brette, F. and Orchard, C. (2003) Circ. Res. 92:1182-1192; Marks, A. R. (2013) J. Clin. Invest. 123:46-52), ability to generate force comparable to other studies of engineered ventricular tissue, loss of automaticity, and acquisition of adult-rod shaped ventricular cardiomyocytes.

After 5 months post-transplantation of purified HVPs, no tumors formed in all of our animals. Animals were sacrificed and the engrafted kidneys were removed for further analysis. The 5-month human graft was a hemisphere structure with the radius of 0.4 cm (diameter of 0.8 cm). The volume for the 5-month human graft was around 0.13 cm³ for one kidney, a volume that suggests feasibility for generating human ventricular muscle that achieves a thickness comparable to the in vivo human adult heart. Rod-shaped mature human ventricular myocytes were observed in the human muscle organ. In addition, muscle trips taken from our mature human muscle organ generated forces (0.36±0.04 mN) in response to electric stimulation and increased their force generation after treatment with a β-adrenergic agonist isoprenaline (0.51±0.02 mN, p<0.05 compared to control). Taken together, these studies indicate that the HVPs are capable of generating a fully functional, mature human ventricular muscle organ in vivo via a cell autonomous pathway, i.e., without the addition of other cells, genes, matrix proteins, or biomaterials.

Example 9: HVPs Migrate Towards an Epicardial Niche and Spontaneously Form a Human Ventricular Muscle Patch on the Surface of a Normal Murine Heart In Vivo

The epicardium is a known niche for heart progenitors, driving the growth of the ventricular chamber during compact zone expansion, as well as serving as a home to adult epicardial progenitors that can expand after myocardial injury and that can drive vasculogenesis in response to known vascular cell fate switches, such as VEGF (Giordano, F. J. et al. (2001) Proc. Natl. Acad. Sci. USA 98:5780-5785; Masters, M. and Riley, P. R. (2014) Stem Cell Res. 13:683-692; Zangi, L. et al. (2013) Nat. Biotechnol. 31:898-907). To determine if the HVPs might migrate spontaneously to the epicardial surface of the normal heart, purified green fluorescent protein (GFP)-labeled HVPs were injected intra-myocardially into the hearts of immunocompromised mice. After one week or one month post-transplantation, animals were sacrificed and the engrafted hearts were removed for histology. After one week post-transplantation, the majority of GFP+ cells were retained in the myocardium. However, almost all the GFP+ cells migrated to the epicardium after one month post-transplantation. In addition, GFP+ cells were ISL1+ and Ki67+ after one week post-transplantation.

In order to trace the differentiation potential of Islet1+ cells, the purified ISL1+JAG1+ cells generated from a cTnT promoter driven green fluorescent protein (GFP)-expressing hESC line (H9-cTnT-GFP) were transplanted into the hearts of severe combined immunodeficient (SCID) beige mice to document their developmental potential in vivo. One month after transplantation of Isl1+Jag1+ cells directly into the ventricle of the hearts of SCID beige mice, Hematoxylin and eosin staining revealed a human muscle strip graft present in the epicardium of the murine heart. In addition, immunohistological analyses revealed the presence of GFP+ donor cells detected by epifluorescence and by staining with an anti-GFP antibody. More importantly, when analysed with antibodies of MLC2v and MLC2a, the grafted human muscle strip is positive for MLC2v (100% of cells +), and negative for the atrial marker MLC2a, indicating the transplanted ISL1+ cells not only further differentiated to cardiac muscle cells, but also became ventricular muscle cells.

Taken together, these studies indicate that the HNPs can migrate to an epicardial niche. where they expand, and subsequently differentiate in to a homogenous ventricular muscle patch, again without the addition of exogenous cells, genes, matrices, or biomaterials.

Example 10: Additional Experimental Materials and Methods

In this example, additional details on the experimental materials and methods used in Examples 1-9 are provided.

Maintenance of hPSCs

hESCs (ES03, H9) and human iPSCs (19-9-11) were maintained on Matrigel (BD Biosciences) coated plates in mTeSR1 medium (STEMCELL Technologies) according to previous published methods (Lian, X. et al. (2013) Nat. Proc. 8:162-175; Lian, X. et al. (2013) Stem Cells 31:447-457).

Human Ventricular Progenitor Generation (HVPG) Protocol

hPSCs maintained on a Matrigel-coated surface in mTeSR1 were dissociated into single cells with Accutase at 37° C. for 10 min and then seeded onto a Matrigel-coated cell culture dish at 100,000-200,000 cell/cm² in mTeSR1 supplemented with 5 μM ROCK inhibitor Y-27632 (day −2) for 24 hours. At day −1, cells were cultured in mTeSR1. At day 0, cells were treated with 1 μM CHIR-98014 (Selleckchem) in RPMI supplemented with B27 minus insulin (RPMI/B27-ins) for 24 hours (day 0 to day 1), which was then removed during the medium change on day 1. At day 3, half of the medium was changed to the RPMI/B27-ins medium containing 2 μM Wnt-059 (Selleckchem), which was then removed during the medium change on day 5. At day 6, cells were dissociated into single cells and purified with anti-JAG1 or anti-FZD4 antibody.

RNA-Seq Library Construction

RNA was isolated (RNeasy Mini kit, Qiagen), quantified (Qubit RNA Assay Kit, Life Technologies) and quality controlled (BioAnalyzer 2100, Agilent). RNA (800 ng) from each sample was used as input for the Illumina TruSeq mRNA Sample Prep Kit v2 (Illumina) and sequencing libraries were created according to the manufacturer's protocol. Briefly, poly-A containing mRNA molecules were purified using poly-T oligo-attached magnetic beads. Following purification, the mRNA was fragmented and copied into first strand complementary DNA using random primers and reverse transcriptase. Second strand cDNA synthesis was then done using DNA polymerase I and RNase H. The cDNA was ligated to adapters and enriched with PCR to create the final cDNA library. The library was pooled and sequenced on a HiSeq 2000 (Illumina) instrument per the manufacturer's instructions.

RNA-Seq Data Processing

The RNA-seq reads were trimmed and mapped to the hg19 reference using Tophat 2. On average, approximately 23 million reads were generated per sample, and 76% of these reads were uniquely mapped. Expression levels for each gene were quantified using the python script rpkmforgenes and annotated using RefSeq. Genes without at least one sample with at least ten reads were removed from the analysis. Principle Component Analysis and heatmaps were constructed using the R and Gene-E respectively.

Transplantation

Aliquots of 2 million purified HVPs were collected into an eppendorf tube. Cells were spun down, and the supernatant was discarded. Each tube of cells was transplanted under the kidney capsule, or intra-myocardially injected into the heart of the immunodeficient mice, NOD.Cg-Prkdcscid Il2rgtm1Wjl/SzJ or SCID-Beige respectively (Charles River France), following a previously described protocol (Shultz, L. D. et al. (2005) J. Immunol. 174:6477-6489). Engrafted Kidneys or hearts are harvested at various time intervals for histological and physiological analysis.

Flow Cytometry

Cells were dissociated into single cells with Accutase for 10 min and then fixed with 1% paraformaldehyde for 20 min at room temperature and stained with primary and secondary antibodies in PBS plus 0.1% Triton X-100 and 0.5% BSA. Data were collected on a FACSCaliber flow cytometer (Beckton Dickinson) and analyzed using FlowJo.

Immunostaining

Cells were fixed with 4% paraformaldehyde for 15 min at room temperature and then stained with primary and secondary antibodies in PBS plus 0.4% Triton X-100 and 5% non-fat dry milk (Bio-Rad). Nuclei were stained with Gold Anti-fade Reagent with DAPI (Invitrogen). An epifluorescence microscope and a confocal microscope (ZEISS, LSM 700) were used for imaging analysis.

Western Blot Analysis

Cells were lysed in M-PER Mammalian Protein Extraction Reagent (Pierce) in the presence of Halt Protease and Phosphatase Inhibitor Cocktail (Pierce). Proteins were separated by 10% Tris-Glycine SDS/PAGE (Invitrogen) under denaturing conditions and transferred to a nitrocellulose membrane. After blocking with 5% dried milk in TBST, the membrane was incubated with primary antibody overnight at 4° C. The membrane was then washed, incubated with an anti-mouse/rabbit peroxidase-conjugated secondary antibody at room temperature for 1 hour, and developed by SuperSignal chemiluminescence (Pierce).

Electrophysiology (Patch Clamping)

Beating ventricular myocyte clusters were microdissected and replated onto glass coverslips before recording. Action potential activity was assessed using borosilicate glass pipettes (4-5 M Ohm resistance) filled with intracellular solution consisting of 120 mM K D-gluconate, 25 mM KCl, 4 mM MgATP, 2 mM NaGTP, 4 mM Na2-phospho-creatin, 10 mM EGTA, 1 mM CaCl2, and 10 mM HEPES (pH 7.4 adjusted with HCl at 25° C.). Cultured cardiomyocytes seeded on coverslip dishes were submerged in extracellular solution (Tyrode's solution) containing 140 mM NaCl, 5.4 mM KCl, 1 mM MgCl2, 10 mM glucose, 1.8 mM CaCl2, and 10 mM HEPES (pH 7.4 adjusted with NaOH at 25° C.). Spontaneous action potentials were recorded at 37° C. using patch clamp technique (whole-cell, current clamp configuration) performed using a Multiclamp 700B amplifier (Molecular Devices, CA, USA) software low-pass filtered at 1 kHz, digitized and stored using a Digidata 1322A and Clampex 9.6 software (Molecular Devices, CA, USA).

Statistics

Data are presented as mean±standard error of the mean (SEM). Statistical significance was determined by Student's t-test (two-tail) between two groups. P<0.05 was considered statistically significant.

Example 11: Xeno-Free Human Ventricular Progenitor Differentiation Protocol

In this example, an alternative differentiation protocol for differentiation of human ventricular progenitors is provided, which utilizes a defined, xeno-free culture medium, Essential 8. The Essential 8 medium was developed for growth and expansion of human pluripotent stem cells (hPSCs) and is described further in Chen, G. et al. (2011) Nat. Methods 8:424-429 (referred to therein as “E8” medium).

hPSCs maintained on a Vitronectin (or Laminin 521)-coated surface in Essential 8 medium were dissociated into single cells with Versene solution at 37° C. for 10 min and then seeded onto a Vitronectin (or Laminin 521)-coated cell culture dish at 100,000-200,000 cell/cm² in Essential 8 medium supplemented with 5 μM ROCK inhibitor Y-27632 (day −2) for 24 hours. At day −1, cells were cultured in Essential 8 medium. At day 0, cells were treated with 0.5 μM CHIR-98014 in RPMI for 24 hours (day 0 to day 1), which was then removed during the medium change on day 1. At day 3, half of the medium was changed to the RPMI medium containing 0.5 μM Wnt-059, which was then removed during the medium change on day 5. At day 6, cells (human ventricular progenitors) were dissociated into single cells and purified with anti-JAG1 or anti-FZD4 antibody. Alternatively cells are purified with anti-LIFR, anti-FGFR3 antibody or anti-TNFSF9 antibody.

Example 12: Angiogenic Markers for Engraftable Human Ventricular Progenitor Cells

In this example, genes in the angiogenic family that are expressed in human ventricular progenitor cells (HVPs) were identified. HVPs were generated as described in Examples 1 or 11 and RNA sequencing (RNA-seq) was performed at different time points following differentiation as described in Example 2. Cluster analysis of gene expression profiles at different time points during HVP differentiation identified stage-specific signature genes. These genes were clustered hierarchically on the basis of the similarity of their expression profiles. First, genes showing expression in four different categories were identified: (i) cell surface expression; (ii) co-expression with Islet 1; (iii) high expression on day 5 of differentiation; and (iv) high d5/d0 ratio. This analysis confirmed the cell surface markers for HVPs of: JAG1, FZD4, FGFR3, LIFR (CD118) and TNFSF9. Next, from this same population of HVPs that identified the cell surface markers, gene ontogeny searches were performed to identify angiogenic family genes that were expressed in this population of HVPs, to thereby identify a gene fingerprint profile that identifies genes critical for cell engraftment.

Statistically, Pearson's correlation with Isl1 expression was used to identify those angiogenic genes whose expression in the HVPs best correlated with Isl1 expression. Table 1 below lists the angiogenic genes that correlate with Isl1 expression with a Pearson's correlation of 0.50 or higher.

TABLE 1 Angiogenic genes expressed in HVPs with a Pearson Correlation with Isl1 Expression of 0.50 or greater Pearson's Correlation with Gene Angiogenic genes (GO:0001525) Isl1 Expression FGF10 fibroblast growth factor 10 0.98 PRKD1 protein kinase D1 0.95 CCBE1 collagen and calcium binding EGF domains 1 0.94 PDGFRA platelet-derived growth factor receptor, alpha polypeptide 0.94 EPHB2 EPH receptor B2 0.92 GATA2 GATA binding protein 2 0.92 NTRK1 neurotrophic tyrosine kinase, receptor, type 1 0.92 PTGIS prostaglandin I2 (prostacyclin) synthase 0.87 BMPER BMP binding endothelial regulator 0.85 BMP4 bone morphogenetic protein 4 0.84 C1GALT1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3- 0.84 beta-galactosyltransferase 1 MEIS1 Meis homeobox 1 0.83 TBX1 T-box 1 0.83 PKNOX1 PBX/knotted 1 homeobox 1 0.83 ID1 inhibitor of DNA binding 1, dominant negative helix-loop- 0.82 helix protein TCF21 transcription factor 21 0.82 HEY1 hes-related family bHLH transcription factor with YRPW 0.80 motif 1 HOXB3 homeobox B3 0.78 JAG1 jagged 1 0.75 HGF hepatocyte growth factor (hepapoietin A; scatter factor) 0.74 IL6 interleukin 6 0.74 GHRL ghrelin/obestatin prepropeptide 0.73 IHH indian hedgehog 0.70 SRPK2 SRSF protein kinase 2 0.70 GATA6 GATA binding protein 6 0.69 HAND1 heart and neural crest derivatives expressed 1 0.69 AMOT angiomotin 0.69 NRP2 neuropilin 2 0.65 PTEN phosphatase and tensin homolog 0.65 SEMA3E sema domain, immunoglobulin domain (Ig), short basic 0.64 domain, secreted, (semaphorin) 3E APOLD1 apolipoprotein L domain containing 1 0.62 SETD2 SET domain containing 2 0.62 DAB2IP DAB2 interacting protein 0.61 KDR kinase insert domain receptor 0.60 PGF placental growth factor 0.60 EMP2 epithelial membrane protein 2 0.59 TAL1 T-cell acute lymphocytic leukemia 1 0.58 ACVR1 activin A receptor, type I 0.58 HIPK2 homeodomain interacting protein kinase 2 0.56 CSPG4 chondroitin sulfate proteoglycan 4 0.55 TNFAIP3 tumor necrosis factor, alpha-induced protein 3 0.55 NRP1 neuropilin 1 0.55 NFATC4 nuclear factor of activated T-cells, cytoplasmic, 0.54 calcineurin-dependent 4 CDC42 cell division cycle 42 0.54 ANGPTL4 angiopoietin-like 4 0.53 BCAS3 breast carcinoma amplified sequence 3 0.53 HIPK1 homeodomain interacting protein kinase 1 0.53 NRXN3 neurexin 3 0.52 FZD5 frizzled class receptor 5 0.52 HHEX hematopoietically expressed homeobox 0.50

Table 2 below lists the angiogenic genes that correlate with Isl1 expression with a Pearson's correlation of 0.49-0.00.

TABLE 2 Angiogenic genes expressed in HVPs with a Pearson Correlation with Isl1 Expression of 0.49 to 0.00 Pearson's Correlation with Gene Angiogenic genes (GO:0001525) Isl1 Expression ACVRL1 activin A receptor type II-like 1 0.49 ENPEP glutamyl aminopeptidase (aminopeptidase A) 0.49 EFNA1 ephrin-A1 0.49 CHRNA7 cholinergic receptor, nicotinic, alpha 7 (neuronal) 0.49 TMEM100 transmembrane protein 100 0.48 NOS3 nitric oxide synthase 3 (endothelial cell) 0.47 LEF1 lymphoid enhancer-binding factor 1 0.47 NRXN1 neurexin 1 0.46 EPHB3 EPH receptor B3 0.44 ROCK1 Rho-associated, coiled-coil containing protein kinase 1 0.42 NF1 neurofibromin 1 0.42 CYSLTR2 cysteinyl leukotriene receptor 2 0.42 FGFR2 fibroblast growth factor receptor 2 0.41 GATA4 GATA binding protein 4 0.40 FMNL3 formin-like 3 0.40 C3 complement component 3 0.40 WASF2 WAS protein family, member 2 0.40 CALCRL calcitonin receptor-like 0.39 HIF1A hypoxia inducible factor 1, alpha subunit (basic helix-loop- 0.39 helix transcription factor) VEGFA vascular endothelial growth factor A 0.39 KRIT1 KRIT1, ankyrin repeat containing 0.39 CDH13 cadherin 13 0.39 COL18A1 collagen, type XVIII, alpha 1 0.39 STK4 serine/threonine kinase 4 0.38 C5 complement component 5 0.38 HDAC7 histone deacetylase 7 0.38 ANGPT2 angiopoietin 2 0.38 PLCG1 phospholipase C, gamma 1 0.37 EDNRA endothelin receptor type A 0.35 TGFB2 transforming growth factor, beta 2 0.35 HAND2 heart and neural crest derivatives expressed 2 0.35 CD34 CD34 molecule 0.35 BTG1 B-cell translocation gene 1, anti-proliferative 0.34 TGFBR1 transforming growth factor, beta receptor 1 0.33 FGFR1 fibroblast growth factor receptor 1 0.33 FN1 fibronectin 1 0.31 TWIST1 twist family bHLH transcription factor 1 0.31 ELK3 ELK3, ETS-domain protein (SRF accessory protein 2) 0.30 THSD7A thrombospondin, type I, domain containing 7A 0.30 RGCC regulator of cell cycle 0.30 PLCD1 phospholipase C, delta 1 0.29 SPARC secreted protein, acidic, cysteine-rich (osteonectin) 0.29 TBX20 T-box 20 0.28 PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic 0.27 subunit alpha MMRN2 multimerin 2 0.27 FOXO4 forkhead box O4 0.26 RAMP2 receptor (G protein-coupled) activity modifying protein 2 0.25 FLT1 fms-related tyrosine kinase 1 0.25 ADRB2 adrenoceptor beta 2, surface 0.25 SLC12A6 solute carrier family 12 (potassium/chloride transporter), 0.25 member 6 ADM adrenomedullin 0.25 NPPB natriuretic peptide B 0.24 SPINK5 serine peptidase inhibitor, Kazal type 5 0.24 MAPK14 mitogen-activated protein kinase 14 0.24 MMP2 matrix metallopeptidase 2 0.24 PTPRM protein tyrosine phosphatase, receptor type, M 0.23 OVOL2 ovo-like zinc finger 2 0.23 CTNNB1 catenin (cadherin-associated protein), beta 1, 88 kDa 0.22 OTULIN OTU deubiquitinase with linear linkage specificity 0.21 B4GALT1 UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, 0.21 polypeptide 1 PDGFRB platelet-derived growth factor receptor, beta polypeptide 0.20 F3 coagulation factor III (thromboplastin, tissue factor) 0.20 PRKCA protein kinase C, alpha 0.20 LRP5 low density lipoprotein receptor-related protein 5 0.20 MAP3K7 mitogen-activated protein kinase kinase kinase 7 0.20 NRCAM neuronal cell adhesion molecule 0.19 MAP2K5 mitogen-activated protein kinase kinase 5 0.18 S1PR1 sphingosine-1-phosphate receptor 1 0.18 NFATC3 nuclear factor of activated T-cells, cytoplasmic, 0.18 calcineurin-dependent 3 TSPAN12 tetraspanin 12 0.18 LAMA5 laminin, alpha 5 0.17 LOXL2 lysyl oxidase-like 2 0.17 ANGPT1 angiopoietin 1 0.17 GTF2I general transcription factor IIi 0.16 E2F8 E2F transcription factor 8 0.16 PDE3B phosphodiesterase 3B, cGMP-inhibited 0.15 SHB Src homology 2 domain containing adaptor protein B 0.14 MYH9 myosin, heavy chain 9, non-muscle 0.14 FZD8 frizzled class receptor 8 0.14 NOV nephroblastoma overexpressed 0.14 SH2D2A SH2 domain containing 2A 0.14 FGF8 fibroblast growth factor 8 (androgen-induced) 0.13 TIE1 tyrosine kinase with immunoglobulin-like and EGF-like 0.13 domains 1 EGLN1 egl-9 family hypoxia-inducible factor 1 0.12 RORA RAR-related orphan receptor A 0.11 MFGE8 milk fat globule-EGF factor 8 protein 0.11 ARHGAP24 Rho GTPase activating protein 24 0.10 ITGA5 integrin, alpha 5 (fibronectin receptor, alpha polypeptide) 0.10 PARVA parvin, alpha 0.10 ADIPOR2 adiponectin receptor 2 0.09 NPR1 natriuretic peptide receptor 1 0.09 ITGB1 integrin, beta 1 (fibronectin receptor, beta polypeptide, 0.09 antigen CD29 includes MDF2, MSK12) HIF3A hypoxia inducible factor 3, alpha subunit 0.08 EPAS1 endothelial PAS domain protein 1 0.08 FOXC2 forkhead box C2 0.07 ANXA2 annexin A2 0.06 RBM15 RNA binding motif protein 15 0.06 PITX2 paired-like homeodomain 2 0.06 FOXC1 forkhead box C1 0.06 SRF serum response factor 0.06 ECSCR endothelial cell surface expressed chemotaxis and 0.05 apoptosis regulator SOX17 SRY (sex determining region Y)-box 17 0.04 HDAC5 histone deacetylase 5 0.04 LRG1 leucine-rich alpha-2-glycoprotein 1 0.04 ADAM8 ADAM metallopeptidase domain 8 0.03 UBP1 upstream binding protein 1 (LBP-1a) 0.02 VASH1 vasohibin 1 0.02 ANXA3 annexin A3 0.01 RRAS related RAS viral (r-ras) oncogene homolog 0.01 TYMP thymidine phosphorylase 0.01 PRCP prolylcarboxypeptidase (angiotensinase C) 0.01 SEMA5A sema domain, seven thrombospondin repeats (type 1 and 0.00 type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A GREM1 gremlin 1, DAN family BMP antagonist 0.00

Angiogenic genes whose expression negatively correlated with Isl1 expression in the HVPs were also identified. Table 3 below lists the angiogenic genes that negatively correlate with Isl1 expression with a Pearson's correlation of −0.50 or less.

TABLE 3 Angiogenic genes expressed in HVPs with a Pearson Correlation with Isl1 Expression of −0.50 or less Pearson's Correlation with Gene Angiogenic genes (GO:0001525) Isl1 Expression ETS1 v-ets avian erythroblastosis virus E26 oncogene homolog 1 −0.50 BAX BCL2-associated X protein −0.50 XBP1 X-box binding protein 1 −0.52 TDGF1 teratocarcinoma-derived growth factor 1 −0.53 C5AR1 complement component 5a receptor 1 −0.53 EPHA1 EPH receptor A1 −0.53 HS6ST1 heparan sulfate 6-O-sulfotransferase 1 −0.56 SHC1 SHC (Src homology 2 domain containing) transforming −0.56 protein 1 SP100 SP100 nuclear antigen −0.58 JAM3 junctional adhesion molecule 3 −0.58 CASP8 caspase 8, apoptosis-related cysteine peptidase −0.60 FLT4 fms-related tyrosine kinase 4 −0.60 SFRP2 secreted frizzled-related protein 2 −0.61 HPSE heparanase −0.61 BAK1 BCL2-antagonist/killer 1 −0.65 GPX1 glutathione peroxidase 1 −0.65 VAV3 vav 3 guanine nucleotide exchange factor −0.70 VAV2 vav 2 guanine nucleotide exchange factor −0.72 EGF epidermal growth factor −0.72 ADAM15 ADAM metallopeptidase domain 15 −0.73 AGGF1 angiogenic factor with G patch and FHA domains 1 −0.76

Table 4 below lists the angiogenic genes that negatively correlate with Isl1 expression with a Pearson's correlation of −0.01 to −0.49

TABLE 4 Angiogenic genes expressed in HVPs with a Pearson Correlation with Isl1 Expression of −0.01 to −0.49 Pearson's Correlation with Gene Angiogenic genes (GO:0001525) Isl1 Expression EIF2AK3 eukaryotic translation initiation factor 2-alpha kinase 3 −0.01 ROCK2 Rho-associated, coiled-coil containing protein kinase 2 −0.01 WNT5A wingless-type MMTV integration site family, member 5A −0.02 NR4A1 nuclear receptor subfamily 4, group A, member 1 −0.02 CYP1B1 cytochrome P450, family 1, subfamily B, polypeptide 1 −0.02 PTK2 protein tyrosine kinase 2 −0.03 SFRP1 secreted frizzled-related protein 1 −0.04 STAT1 signal transducer and activator of transcription 1, 91 kDa −0.04 ITGAV integrin, alpha V −0.04 EPHB4 EPH receptor B4 −0.05 CYR61 cysteine-rich, angiogenic inducer, 61 −0.05 TEK TEK tyrosine kinase, endothelial −0.06 COL15A1 collagen, type XV, alpha 1 −0.06 COL4A1 collagen, type IV, alpha 1 −0.07 ANG angiogenin, ribonuclease, RNase A family, 5 −0.07 HSPB1 heat shock 27 kDa protein 1 −0.07 PLXND1 plexin D1 −0.08 HSPG2 heparan sulfate proteoglycan 2 −0.09 VEGFC vascular endothelial growth factor C −0.09 SYNJ2BP synaptojanin 2 binding protein −0.09 THBS1 thrombospondin 1 −0.09 CTGF connective tissue growth factor −0.10 ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61) −0.12 AAMP angio-associated, migratory cell protein −0.12 GJA5 gap junction protein, alpha 5, 40 kDa −0.12 PRKCB protein kinase C, beta −0.13 EGR3 early growth response 3 −0.13 JMJD6 jumonji domain containing 6 −0.13 TGFBI transforming growth factor, beta-induced, 68 kDa −0.14 SIRT1 sirtuin 1 −0.14 ANGPTL3 angiopoietin-like 3 −0.14 ACKR3 atypical chemokine receptor 3 −0.14 SAT1 spermidine/spermine N1-acetyltransferase 1 −0.15 VEGFB vascular endothelial growth factor B −0.16 UTS2 urotensin 2 −0.16 JUN jun proto-oncogene −0.16 TNFSF12 tumor necrosis factor (ligand) superfamily, member 12 −0.16 EGFL7 EGF-like-domain, multiple 7 −0.17 MED1 mediator complex subunit 1 −0.17 SLIT2 slit guidance ligand 2 −0.17 SERPINF1 serpin peptidase inhibitor, clade F (alpha-2 antiplasmin, −0.18 pigment epithelium derived factor), member 1 NOTCH3 notch 3 −0.18 FGF9 fibroblast growth factor 9 −0.19 DLL4 delta-like 4 (Drosophila) −0.19 CCL2 chemokine (C-C motif) ligand 2 −0.19 MMP14 matrix metallopeptidase 14 (membrane-inserted) −0.19 TMPRSS6 transmembrane protease, serine 6 −0.19 EPGN epithelial mitogen −0.20 RBPJ recombination signal binding protein for immunoglobulin −0.20 kappa J region COL4A2 collagen, type IV, alpha 2 −0.20 PRKD2 protein kinase D2 −0.20 ALOX12 arachidonate 12-lipoxygenase −0.21 RNH1 ribonuclease/angiogenin inhibitor 1 −0.21 APOH apolipoprotein H (beta-2-glycoprotein I) −0.21 CHI3L1 chitinase 3-like 1 (cartilage glycoprotein-39) −0.21 ESM1 endothelial cell-specific molecule 1 −0.22 PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H −0.22 synthase and cyclooxygenase) ANPEP alanyl (membrane) aminopeptidase −0.22 LEMD3 LEM domain containing 3 −0.22 UTS2R urotensin 2 receptor −0.22 CIB1 calcium and integrin binding 1 (calmyrin) −0.22 ITGB1BP1 integrin beta 1 binding protein 1 −0.22 AQP1 aquaporin 1 (Colton blood group) −0.22 IL18 interleukin 18 −0.22 EPHA2 EPH receptor A2 −0.22 EPHB1 EPH receptor B1 −0.22 AGT angiotensinogen (serpin peptidase inhibitor, clade A, −0.22 member 8) PLAU plasminogen activator, urokinase −0.22 VEZF1 vascular endothelial zinc finger 1 −0.23 SPHK1 sphingosine kinase 1 −0.23 SRPX2 sushi-repeat containing protein, X-linked 2 −0.23 PDCL3 phosducin-like 3 −0.23 COL8A1 collagen, type VIII, alpha 1 −0.24 HDAC9 histone deacetylase 9 −0.24 CTSH cathepsin H −0.24 EDN1 endothelin 1 −0.24 CXCL8 chemokine (C-X-C motif) ligand 8 −0.24 ECM1 extracellular matrix protein 1 −0.24 BRCA1 breast cancer 1, early onset −0.24 EFNB2 ephrin-B2 −0.25 SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen −0.25 activator inhibitor type 1), member 1 SASH1 SAM and SH3 domain containing 1 −0.25 WNT7B wingless-type MMTV integration site family, member 7B −0.25 RAMP1 receptor (G protein-coupled) activity modifying protein 1 −0.26 SCG2 secretogranin II −0.26 COL8A2 collagen, type VIII, alpha 2 −0.26 SULF1 sulfatase 1 −0.26 CLIC4 chloride intracellular channel 4 −0.26 FGF1 fibroblast growth factor 1 (acidic) −0.27 NODAL nodal growth differentiation factor −0.27 RASIP1 Ras interacting protein 1 −0.28 RLN2 relaxin 2 −0.28 POFUT1 protein O-fucosyltransferase 1 −0.28 FGF18 fibroblast growth factor 18 −0.28 AIMP1 aminoacyl tRNA synthetase complex-interacting −0.28 multifunctional protein 1 TGFBR2 transforming growth factor, beta receptor II (70/80 kDa) −0.28 RHOB ras homolog family member B −0.28 GBX2 gastrulation brain homeobox 2 −0.28 ENPP2 ectonucleotide pyrophosphatase/phosphodiesterase 2 −0.29 MAPK7 mitogen-activated protein kinase 7 −0.30 PROK2 prokineticin 2 −0.30 E2F7 E2F transcription factor 7 −0.30 ERAP1 endoplasmic reticulum aminopeptidase 1 −0.31 MTDH metadherin −0.31 KLF5 Kruppel-like factor 5 (intestinal) −0.31 DICER1 dicer 1, ribonuclease type III −0.32 LECT1 leukocyte cell derived chemotaxin 1 −0.32 CX3CL1 chemokine (C-X3-C motif) ligand 1 −0.32 PTK2B protein tyrosine kinase 2 beta −0.33 SEMA4A sema domain, immunoglobulin domain (Ig), −0.34 transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A ARHGAP22 Rho GTPase activating protein 22 −0.34 RSPO3 R-spondin 3 −0.34 KLF4 Kruppel-like factor 4 (gut) −0.34 ROBO1 roundabout guidance receptor 1 −0.34 GPLD1 glycosylphosphatidylinositol specific phospholipase D1 −0.35 NUS1 NUS1 dehydrodolichyl diphosphate synthase subunit −0.35 NRARP NOTCH-regulated ankyrin repeat protein −0.35 PDCD10 programmed cell death 10 −0.36 PF4 platelet factor 4 −0.36 PRKX protein kinase, X-linked −0.36 PML promyelocytic leukemia −0.36 ATP5B ATP synthase, H+ transporting, mitochondrial F1 complex, −0.36 beta polypeptide TNFRSF12A tumor necrosis factor receptor superfamily, member 12A −0.36 ENG endoglin −0.37 THY1 Thy-1 cell surface antigen −0.37 FGF2 fibroblast growth factor 2 (basic) −0.37 CXCL12 chemokine (C-X-C motif) ligand 12 −0.37 CAV1 caveolin 1, caveolae protein, 22 kDa −0.38 PDGFA platelet-derived growth factor alpha polypeptide −0.38 PNPLA6 patatin-like phospholipase domain containing 6 −0.38 PLCD3 phospholipase C, delta 3 −0.38 DDAH1 dimethylarginine dimethylaminohydrolase 1 −0.39 GNA13 guanine nucleotide binding protein (G protein), alpha 13 −0.39 ADM2 adrenomedullin 2 −0.39 HMOX1 heme oxygenase 1 −0.40 MCAM melanoma cell adhesion molecule −0.41 RAPGEF3 Rap guanine nucleotide exchange factor (GEF) 3 −0.41 TNFAIP2 tumor necrosis factor, alpha-induced protein 2 −0.41 HTATIP2 HIV-1 Tat interactive protein 2, 30 kDa −0.42 NCL nucleolin −0.42 ERBB2 erb-b2 receptor tyrosine kinase 2 −0.43 NAA15 N(alpha)-acetyltransferase 15, NatA auxiliary subunit −0.43 ATPIF1 ATPase inhibitory factor 1 −0.43 THBS4 thrombospondin 4 −0.43 SYK spleen tyrosine kinase −0.44 LIF leukemia inhibitory factor −0.44 THBS2 thrombospondin 2 −0.44 PPP1R16B protein phosphatase 1, regulatory subunit 16B −0.44 NOTCH1 notch 1 −0.44 RUNX1 runt-related transcription factor 1 −0.45 PDCD6 programmed cell death 6 −0.45 VASH2 vasohibin 2 −0.45 GPI glucose-6-phosphate isomerase −0.46 ZC3H12A zinc finger CCCH-type containing 12A −0.46 WARS tryptophanyl-tRNA synthetase −0.46 HYAL1 hyaluronoglucosaminidase 1 −0.47 PIK3CB phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic −0.47 subunit beta TNMD tenomodulin −0.49

Example 13: Extracellular Matrix Markers for Engraftable Human Ventricular Progenitor Cells

In this example, genes in the extracellular matrix family that are expressed in human ventricular progenitor cells (HVPs) were identified. HVPs were generated as described in Examples 1 or 11 and RNA sequencing (RNA-seq) was performed at different time points following differentiation as described in Example 2. Cluster analysis of gene expression profiles at different time points during HVP differentiation identified stage-specific signature genes. These genes were clustered hierarchically on the basis of the similarity of their expression profiles. First, genes showing expression in four different categories were identified: (i) cell surface expression; (ii) co-expression with Islet 1; (iii) high expression on day 5 of differentiation; and (iv) high d5/d0 ratio. This analysis confirmed the cell surface markers for HVPs of: JAG1, FZD4, FGFR3, LIFR (CD118) and TNFSF9. Next, from this same population of HVPs that identified the cell surface markers, gene ontogeny searches were performed to identify extracellular matrix family genes that were expressed in this population of HVPs, to thereby identify a gene fingerprint profile that identifies genes critical for cell engraftment.

Statistically, Pearson's correlation with Isl1 expression was used to identify those extracellular matrix genes whose expression in the HVPs best correlated with Isl1 expression. Table 5 below lists the extracellular matrix genes that correlate with Isl1 expression with a Pearson's correlation of 0.50 or higher.

TABLE 5 Extracellular matrix genes expressed in HVPs with a Pearson Correlation with Isl1 Expression of 0.50 or greater Pearson's Correlation with Gene Extracellular matrix genes (GO:0031012) Isl1 Expression FGF10 fibroblast growth factor 10 0.98 SMOC1 SPARC related modular calcium binding 1 0.97 CCBE1 collagen and calcium binding EGF domains 1 0.94 COL6A6 collagen, type VI, alpha 6 0.89 ADAMTS12 ADAM metallopeptidase with thrombospondin type 1 0.85 motif, 12 COL19A1 collagen, type XIX, alpha 1 0.85 LAMA1 laminin, alpha 1 0.85 BMP4 bone morphogenetic protein 4 0.84 FBLN7 fibulin 7 0.81 FBLN2 fibulin 2 0.81 NDNF neuron-derived neurotrophic factor 0.80 HTRA1 HtrA serine peptidase 1 0.80 HAPLN1 hyaluronan and proteoglycan link protein 1 0.79 EMILIN1 elastin microfibril interfacer 1 0.79 SPOCK3 sparc/osteonectin, cwcv and kazal-like domains 0.76 proteoglycan (testican) 3 PODNL1 podocan-like 1 0.73 IHH indian hedgehog 0.70 ACAN aggrecan 0.69 NID2 nidogen 2 (osteonidogen) 0.69 COL4A6 collagen, type IV, alpha 6 0.68 LAMC1 laminin, gamma 1 (formerly LAMB2) 0.65 FMOD fibromodulin 0.65 MUC4 mucin 4, cell surface associated 0.64 EMID1 EMI domain containing 1 0.62 HMCN1 hemicentin 1 0.61 NID1 nidogen 1 0.60 VCAN versican 0.58 CILP2 cartilage intermediate layer protein 2 0.57 SOD3 superoxide dismutase 3, extracellular 0.56 ADAMTS3 ADAM metallopeptidase with thrombospondin type 1 0.54 motif, 3 ZP3 zona pellucida glycoprotein 3 (sperm receptor) 0.54 ANGPTL4 angiopoietin-like 4 0.53 CRTAC1 cartilage acidic protein 1 0.52 LTBP4 latent transforming growth factor beta binding protein 4 0.50 FREM1 FRAS1 related extracellular matrix 1 0.50

Table 6 below lists the extracellular matrix genes that correlate with Isl1 expression with a Pearson's correlation of 0.49-0.00.

TABLE 6 Extracellular matrix genes expressed in HVPs with a Pearson Correlation with Isl1 Expression of 0.49 to 0.00 Pearson's Correlation with Gene Extracellular matrix genes (GO:0031012) Isl1 Expression SSC5D scavenger receptor cysteine rich family, 5 domains 0.49 GPC6 glypican 6 0.49 COL1A1 collagen, type I, alpha 1 0.49 ADAMTSL3 ADAMTS-like 3 0.48 FLRT3 fibronectin leucine rich transmembrane protein 3 0.48 FBLN1 fibulin 1 0.48 ADAMTS9 ADAM metallopeptidase with thrombospondin type 1 0.48 motif, 9 COL27A1 collagen, type XXVII, alpha 1 0.47 RELN reelin 0.46 COL9A2 collagen, type IX, alpha 2 0.46 EFEMP2 EGF containing fibulin-like extracellular matrix protein 2 0.45 AGRN agrin 0.44 PCOLCE procollagen C-endopeptidase enhancer 0.44 NTN4 netrin 4 0.44 CD248 CD248 molecule, endosialin 0.44 TGFB1 transforming growth factor, beta 1 0.43 ADAMTS2 ADAM metallopeptidase with thrombospondin type 1 0.43 motif, 2 CTHRC1 collagen triple helix repeat containing 1 0.42 FGFR2 fibroblast growth factor receptor 2 0.41 APOE apolipoprotein E 0.41 MMP11 matrix metallopeptidase 11 0.41 MMP15 matrix metallopeptidase 15 (membrane-inserted) 0.41 PODN podocan 0.39 VEGFA vascular endothelial growth factor A 0.39 COL18A1 collagen, type XVIII, alpha 1 0.39 GLG1 golgi glycoprotein 1 0.39 GPC2 glypican 2 0.37 DAG1 dystroglycan 1 (dystrophin-associated glycoprotein 1) 0.35 TGFB2 transforming growth factor, beta 2 0.35 PRELP proline/arginine-rich end leucine-rich repeat protein 0.35 CHAD chondroadherin 0.33 COL2A1 collagen, type II, alpha 1 0.33 FN1 fibronectin 1 0.31 SMC3 structural maintenance of chromosomes 3 0.31 COL4A5 collagen, type IV, alpha 5 0.30 FBN3 fibrillin 3 0.30 MMP23B matrix metallopeptidase 23B 0.30 CCDC80 coiled-coil domain containing 80 0.29 SPARC secreted protein, acidic, cysteine-rich (osteonectin) 0.29 TNXB tenascin XB 0.28 COL6A2 collagen, type VI, alpha 2 0.28 ADAMTS13 ADAM metallopeptidase with thrombospondin type 1 0.28 motif, 13 LOXL1 lysyl oxidase-like 1 0.28 HAPLN2 hyaluronan and proteoglycan link protein 2 0.28 TNC tenascin C 0.28 ENTPD2 ectonucleoside triphosphate diphosphohydrolase 2 0.28 TGFB3 transforming growth factor, beta 3 0.28 MFAP4 microfibrillar-associated protein 4 0.27 VWF von Willebrand factor 0.27 WNT2 wingless-type MMTV integration site family member 2 0.27 MMRN2 multimerin 2 0.27 SPON1 spondin 1, extracellular matrix protein 0.26 ADAMTS1 ADAM metallopeptidase with thrombospondin type 1 0.26 motif, 1 F2 coagulation factor II (thrombin) 0.26 FLRT2 fibronectin leucine rich transmembrane protein 2 0.25 MMP2 matrix metallopeptidase 2 0.24 COL26A1 collagen, type XXVI, alpha 1 0.24 CASK calcium/calmodulin-dependent serine protein kinase 0.24 (MAGUK family) NTN3 netrin 3 0.23 SLC1A3 solute carrier family 1 (glial high affinity glutamate 0.22 transporter), member 3 F3 coagulation factor III (thromboplastin, tissue factor) 0.20 ADAMTS6 ADAM metallopeptidase with thrombospondin type 1 0.20 motif, 6 COL5A2 collagen, type V, alpha 2 0.19 ERBB2IP erbb2 interacting protein 0.18 LAMB1 laminin, beta 1 0.18 COLQ collagen-like tail subunit (single strand of homotrimer) of 0.18 asymmetric acetylcholinesterase LAMA5 laminin, alpha 5 0.17 LOXL2 lysyl oxidase-like 2 0.17 WNT11 wingless-type MMTV integration site family, member 11 0.17 LAMB2 laminin, beta 2 (laminin S) 0.17 COL5A1 collagen, type V, alpha 1 0.17 AEBP1 AE binding protein 1 0.17 COL9A3 collagen, type IX, alpha 3 0.16 CTSD cathepsin D 0.16 COL21A1 collagen, type XXI, alpha 1 0.16 EGFLAM EGF-like, fibronectin type III and laminin G domains 0.16 FBN2 fibrillin 2 0.15 NAV2 neuron navigator 2 0.15 EMILIN2 elastin microfibril interfacer 2 0.14 WNT9B wingless-type MMTV integration site family, member 9B 0.14 NOV nephroblastoma overexpressed 0.14 CHL1 cell adhesion molecule L1-like 0.13 DLG1 discs, large homolog 1 (Drosophila) 0.11 MFGE8 milk fat globule-EGF factor 8 protein 0.11 TIMP1 TIMP metallopeptidase inhibitor 1 0.11 CST3 cystatin C 0.10 APLP1 amyloid beta (A4) precursor-like protein 1 0.10 PRTN3 proteinase 3 0.10 ADAMTS10 ADAM metallopeptidase with thrombospondin type 1 0.09 motif, 10 ILK integrin-linked kinase 0.09 FRAS1 Fraser extracellular matrix complex subunit 1 0.09 ANXA2P2 annexin A2 pseudogene 2 0.08 SMOC2 SPARC related modular calcium binding 2 0.07 ANXA2 annexin A2 0.06 ODAM odontogenic, ameloblast asssociated 0.06 FREM2 FRAS1 related extracellular matrix protein 2 0.05 HAPLN3 hyaluronan and proteoglycan link protein 3 0.05 GPC3 glypican 3 0.03 LGALS1 lectin, galactoside-binding, soluble, 1 0.02 ADAMTS8 ADAM metallopeptidase with thrombospondin type 1 0.02 motif, 8 LUM lumican 0.01 HSP90B1 heat shock protein 90 kDa beta (Grp94), member 1 0.00 HAPLN4 hyaluronan and proteoglycan link protein 4 0.00 MATN2 matrilin 2 0.00

Extracellular matrix genes whose expression negatively correlated with Isl1 expression in the HVPs were also identified. Table 7 below lists the extracellular matrix genes that negatively correlate with Isl1 expression with a Pearson's correlation of −0.50 or less.

TABLE 7 Extracellular matrix genes expressed in HVPs with a Pearson Correlation with Isl1 Expression of −0.50 or less Pearson's Correlation with Gene Extracellular matrix genes (GO:0031012) Isl1 Expression FKBP1A FK506 binding protein 1A, 12 kDa −0.51 CLU clusterin −0.52 TFPI2 tissue factor pathway inhibitor 2 −0.52 PLSCR1 phospholipid scramblase 1 −0.53 FBLN5 fibulin 5 −0.53 VWA1 von Willebrand factor A domain containing 1 −0.54 ADAMTS16 ADAM metallopeptidase with thrombospondin type 1 −0.55 motif, 16 MMP25 matrix metallopeptidase 25 −0.55 SFRP2 secreted frizzled-related protein 2 −0.61 SOD1 superoxide dismutase 1, soluble −0.68

Table 8 below lists the extracellular matrix genes that negatively correlate with Isl1 expression with a Pearson's correlation of −0.01 to −0.49.

TABLE 8 Extracellular matrix genes expressed in HVPs with a Pearson Correlation with Isl1 Expression of −0.01 to −0.49 Pearson's Correlation with Gene Extracellular matrix genes (GO:0031012) Isl1 Expression PAPLN papilin, proteoglycan-like sulfated glycoprotein −0.01 SOST sclerostin −0.01 CDON cell adhesion associated, oncogene regulated −0.02 HMCN2 hemicentin 2 −0.02 WNT5A wingless-type MMTV integration site family, member 5A −0.02 PCSK6 proprotein convertase subtilisin/kexin type 6 −0.02 GSTO1 glutathione S-transferase omega 1 −0.02 LTBP1 latent transforming growth factor beta binding protein 1 −0.03 KAZALD1 Kazal-type serine peptidase inhibitor domain 1 −0.03 LTBP2 latent transforming growth factor beta binding protein 2 −0.03 SFRP1 secreted frizzled-related protein 1 −0.04 ADAM11 ADAM metallopeptidase domain 11 −0.05 COL6A1 collagen, type VI, alpha 1 −0.05 COL22A1 collagen, type XXII, alpha 1 −0.05 CYR61 cysteine-rich, angiogenic inducer, 61 −0.05 ELN elastin −0.06 COL9A1 collagen, type IX, alpha 1 −0.06 VTN vitronectin −0.06 COL15A1 collagen, type XV, alpha 1 −0.06 COL4A1 collagen, type IV, alpha 1 −0.07 ANG angiogenin, ribonuclease, RNase A family, 5 −0.07 HSPG2 heparan sulfate proteoglycan 2 −0.09 CRIP2 cysteine-rich protein 2 −0.09 CD151 CD151 molecule (Raph blood group) −0.09 THBS1 thrombospondin 1 −0.09 ADAMTS4 ADAM metallopeptidase with thrombospondin type 1 −0.09 motif, 4 CTGF connective tissue growth factor −0.10 CRISPLD2 cysteine-rich secretory protein LCCL domain containing 2 −0.10 BMP7 bone morphogenetic protein 7 −0.11 COL6A3 collagen, type VI, alpha 3 −0.11 COL3A1 collagen, type III, alpha 1 −0.11 COL14A1 collagen, type XIV, alpha 1 −0.11 MATN3 matrilin 3 −0.11 CPZ carboxypeptidase Z −0.11 BMP1 bone morphogenetic protein 1 −0.11 WISP1 WNT1 inducible signaling pathway protein 1 −0.12 ADAMTS18 ADAM metallopeptidase with thrombospondin type 1 −0.12 motif, 18 COL7A1 collagen, type VII, alpha 1 −0.12 IGFBP7 insulin-like growth factor binding protein 7 −0.12 COCH cochlin −0.13 ADAMTS5 ADAM metallopeptidase with thrombospondin type 1 −0.13 motif, 5 COL11A2 collagen, type XI, alpha 2 −0.13 TGFBI transforming growth factor, beta-induced, 68 kDa −0.14 COL16A1 collagen, type XVI, alpha 1 −0.14 ACHE acetylcholinesterase (Yt blood group) −0.14 THSD4 thrombospondin, type I, domain containing 4 −0.15 DGCR6 DiGeorge syndrome critical region gene 6 −0.15 TGFB1I1 transforming growth factor beta 1 induced transcript 1 −0.15 ADAMTSL1 ADAMTS-like 1 −0.15 SERPINA1 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, −0.16 antitrypsin), member 1 MAMDC2 MAM domain containing 2 −0.16 LAMA4 laminin, alpha 4 −0.17 LTBP3 latent transforming growth factor beta binding protein 3 −0.17 EGFL7 EGF-like-domain, multiple 7 −0.17 NPNT nephronectin −0.17 SERPINF1 serpin peptidase inhibitor, clade F (alpha-2 antiplasmin, −0.18 pigment epithelium derived factor), member 1 ABI3BP ABI family, member 3 (NESH) binding protein −0.18 SERPINE2 serpin peptidase inhibitor, clade E (nexin, plasminogen −0.18 activator inhibitor type 1), member 2 WNT6 wingless-type MMTV integration site family, member 6 −0.19 TIMP3 TIMP metallopeptidase inhibitor 3 −0.19 SNCA synuclein, alpha (non A4 component of amyloid precursor) −0.19 PKM pyruvate kinase, muscle −0.19 FGF9 fibroblast growth factor 9 −0.19 VIT vitrin −0.19 WNT1 wingless-type MMTV integration site family, member 1 −0.19 LAMC3 laminin, gamma 3 −0.19 MMP14 matrix metallopeptidase 14 (membrane-inserted) −0.19 PXDN peroxidasin −0.19 HNRNPM heterogeneous nuclear ribonucleoprotein M −0.19 FBN1 fibrillin 1 −0.20 ASPN asporin −0.20 ADAMTSL5 ADAMTS-like 5 −0.20 SPON2 spondin 2, extracellular matrix protein −0.20 COL1A2 collagen, type I, alpha 2 −0.20 BGN biglycan −0.20 COL4A2 collagen, type IV, alpha 2 −0.20 ADAMTSL4 ADAMTS-like 4 −0.21 APOH apolipoprotein H (beta-2-glycoprotein I) −0.21 CHI3L1 chitinase 3-like 1 (cartilage glycoprotein-39) −0.21 ADAMTS7 ADAM metallopeptidase with thrombospondin type 1 −0.22 motif, 7 CALR calreticulin −0.22 MMP9 matrix metallopeptidase 9 −0.22 MMP24 matrix metallopeptidase 24 (membrane-inserted) −0.22 SPOCK2 sparc/osteonectin, cwcv and kazal-like domains −0.22 proteoglycan (testican) 2 COL11A1 collagen, type XI, alpha 1 −0.23 MMP7 matrix metallopeptidase 7 −0.23 MMP16 matrix metallopeptidase 16 (membrane-inserted) −0.23 MFAP2 microfibrillar-associated protein 2 −0.23 POSTN periostin, osteoblast specific factor −0.24 COL8A1 collagen, type VIII, alpha 1 −0.24 WNT2B wingless-type MMTV integration site family, member 2B −0.24 DCN decorin −0.24 EGFL6 EGF-like-domain, multiple 6 −0.24 MMP10 matrix metallopeptidase 10 −0.24 MGP matrix Gla protein −0.24 ECM1 extracellular matrix protein 1 −0.24 SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen −0.25 activator inhibitor type 1), member 1 MMP1 matrix metallopeptidase 1 −0.25 WNT10A wingless-type MMTV integration site family, member 10A −0.25 B4GALT7 xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7 −0.25 COL12A1 collagen, type XII, alpha 1 −0.25 LAMA3 laminin, alpha 3 −0.25 LAMA2 laminin, alpha 2 −0.25 LAMB3 laminin, beta 3 −0.25 WNT7B wingless-type MMTV integration site family, member 7B −0.25 FLRT1 fibronectin leucine rich transmembrane protein 1 −0.25 ADAMTS15 ADAM metallopeptidase with thrombospondin type 1 −0.26 motif, 15 COL8A2 collagen, type VIII, alpha 2 −0.26 MFAP1 microfibrillar-associated protein 1 −0.26 TINAGL1 tubulointerstitial nephritis antigen-like 1 −0.26 FGF1 fibroblast growth factor 1 (acidic) −0.27 OLFML2A olfactomedin-like 2A −0.27 CPA6 carboxypeptidase A6 −0.27 COL17A1 collagen, type XVII, alpha 1 −0.27 SPARCL1 SPARC-like 1 (hevin) −0.27 MFAP5 microfibrillar associated protein 5 −0.27 COL4A4 collagen, type IV, alpha 4 −0.28 WNT8B wingless-type MMTV integration site family, member 8B −0.28 ADAMTS19 ADAM metallopeptidase with thrombospondin type 1 −0.29 motif, 19 CRTAP cartilage associated protein −0.29 WNT5B wingless-type MMTV integration site family, member 5B −0.30 WNT3 wingless-type MMTV integration site family, member 3 −0.30 UCMA upper zone of growth plate and cartilage matrix associated −0.30 GPC1 glypican 1 −0.30 TIMP2 TIMP metallopeptidase inhibitor 2 −0.30 ALPL alkaline phosphatase, liver/bone/kidney −0.30 LECT1 leukocyte cell derived chemotaxin 1 −0.32 GPC4 glypican 4 −0.32 SPOCK1 sparc/osteonectin, cwcv and kazal-like domains −0.32 proteoglycan (testican) 1 HSD17B12 hydroxysteroid (17-beta) dehydrogenase 12 −0.32 LGALS3 lectin, galactoside-binding, soluble, 3 −0.33 EMILIN3 elastin microfibril interfacer 3 −0.34 GFOD2 glucose-fructose oxidoreductase domain containing 2 −0.34 VWC2 von Willebrand factor C domain containing 2 −0.34 SERAC1 serine active site containing 1 −0.34 WNT8A wingless-type MMTV integration site family, member 8A −0.34 LMCD1 LIM and cysteine-rich domains 1 −0.34 CPXM2 carboxypeptidase X (M14 family), member 2 −0.34 ADAMTS14 ADAM metallopeptidase with thrombospondin type 1 −0.34 motif, 14 GPLD1 glycosylphosphatidylinositol specific phospholipase D1 −0.35 FGFBP3 fibroblast growth factor binding protein 3 −0.35 BCAN brevican −0.35 ITGB4 integrin, beta 4 −0.35 LGALS3BP lectin, galactoside-binding, soluble, 3 binding protein −0.36 LPL lipoprotein lipase −0.38 LAD1 ladinin 1 −0.39 WNT3A wingless-type MMTV integration site family, member 3A −0.39 TGFBR3 transforming growth factor, beta receptor III −0.39 DST dystonin −0.40 WNT10B wingless-type MMTV integration site family, member 10B −0.40 LEFTY2 left-right determination factor 2 −0.41 TNFRSF11B tumor necrosis factor receptor superfamily, member 11b −0.41 WNT9A wingless-type MMTV integration site family, member 9A −0.41 TIMP4 TIMP metallopeptidase inhibitor 4 −0.42 WNT4 wingless-type MMTV integration site family, member 4 −0.42 NCAN neurocan −0.42 ADAMTS20 ADAM metallopeptidase with thrombospondin type 1 −0.43 motif, 20 ITGA6 integrin, alpha 6 −0.43 LOX lysyl oxidase −0.43 THBS4 thrombospondin 4 −0.43 THBS2 thrombospondin 2 −0.44 ADAMTSL2 ADAMTS-like 2 −0.44 ENTPD1 ectonucleoside triphosphate diphosphohydrolase 1 −0.45 RUNX1 runt-related transcription factor 1 −0.45 VWA2 von Willebrand factor A domain containing 2 −0.45 RELL2 RELT-like 2 −0.46 PTPRZ1 protein tyrosine phosphatase, receptor-type, Z polypeptide 1 −0.46 LAMC2 laminin, gamma 2 −0.46 DST dystonin −0.40 WNT10B wingless-type MMTV integration site family, member 10B −0.40 LEFTY2 left-right determination factor 2 −0.41 TNFRSF11B tumor necrosis factor receptor superfamily, member 11b −0.41 WNT9A wingless-type MMTV integration site family, member 9A −0.41 TIMP4 TIMP metallopeptidase inhibitor 4 −0.42

Example 14: Gene Expression Profile for Day 6 Islet 1 Negative Cells

In this example, the gene expression profile was determined for Islet 1 negative cells within the Day 6 HVP population to further characterize a subpopulation of cells within the Day 6 population that do not express the necessary markers to qualify as engraftable HVPs. Day 6 HVP populations were generated as described in Examples 1 or 11 and RNA sequencing (RNA-seq) was performed following differentiation as described in Example 2. Cells that were Islet 1 negative (Isl1−) were further analyzed with respect to their gene expression profile. Genes expressed in the Isl1− cells with an average RNA copy number of 2000 or higher are shown below in Table 9.

TABLE 9 Gene Expression Profile of Day 6 Islet 1 Negative Cells Gene Sample #1 Sample #2 Avg. RNA Copy # ACTB 12288 28126 20207 MTRNR2L2 24511 9774 17142.5 MALAT1 14163 18092 16127.5 EEF1A1 11663 12456 12059.5 KRT8 8884 14087 11485.5 MTRNR2L8 12836 7688 10262 KRT18 5215 10552 7883.5 FN1 4900 10581 7740.5 MTRNR2L1 8550 5719 7134.5 TTN 3149 9601 6375 GAPDH 4907 6391 5649 YWHAZ 5349 5414 5381.5 MTRNR2L9 5673 3850 4761.5 RPL3 3346 5911 4628.5 AHNAK 6727 2197 4462 KCNQ1OT1 5835 3064 4449.5 TUBB 4870 3936 4403 SLC2A3 3311 4301 3806 FTL 3484 4021 3752.5 HSP90B1 4173 2778 3475.5 KRT19 3502 3202 3352 HSPA8 3455 2903 3179 MYL6 1898 4375 3136.5 RPLP0 2319 3922 3120.5 BSG 2519 3593 3056 COL3A1 5312 695 3003.5 TPM1 2938 3059 2998.5 VCAN 2563 3422 2992.5 ENO1 2449 3535 2992 RPL4 2619 3328 2973.5 ACTG1 2687 3253 2970 MTRNR2L10 3409 2487 2948 HMGN2 2684 3153 2918.5 PRTG 2594 2980 2787 TPI1 2418 3113 2765.5 HMGB1 2577 2880 2728.5 VIM 2621 2704 2662.5 ATP5B 3000 2219 2609.5 HSP90AB1 2735 2419 2577 RPL7 2132 2896 2514 CBX5 2799 2219 2509 MYL7 1614 3382 2498 SERPINH1 2547 2327 2437 HNRNPK 2878 1932 2405 SRRM2 2758 2046 2402 PODXL 3683 1112 2397.5 EEF2 2579 2119 2349 SPARC 3026 1645 2335.5 ACTC1 437 4152 2294.5 HUWE1 2583 1977 2280 COL1A2 3544 941 2242.5 LINC00506 2965 1496 2230.5 HSPA5 2078 2356 2217 MDK 2223 2144 2183.5 HNRNPC 2292 2074 2183 HSP90AA1 2220 2138 2179 RGS5 2180 2150 2165 LAMC1 2757 1565 2161 APLNR 868 3246 2057 UGDH-AS1 2633 1457 2045 RPS3A 1601 2399 2000

Accordingly, the data shown in Table 9 provides a gene expression profile for Islet 1 negative, non-engraftable cells within a Day 6 HVP population that are not suitable for transplantation and thus are to be selected against when choosing cells for transplantation and engraftment.

EQUIVALENTS

Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents of the specific embodiments of the invention described herein. Such equivalents are intended to be encompassed by the following claims. 

1.-5. (canceled)
 6. The method of claim 31, wherein the at least one engraftment marker detected is at least one positive angiogenic marker.
 7. The method of claim 6, wherein three or more positive angiogenic markers are detected.
 8. The method of claim 6, wherein ten or more positive angiogenic markers are detected.
 9. The method of claim 31, wherein the at least one engraftment marker detected is at least one positive extracellular matrix marker.
 10. The method of claim 9, wherein three or more positive extracellular matrix markers are detected.
 11. The method of claim 9, wherein ten or more positive extracellular matrix markers are detected.
 12. The method of claim 31, wherein the at least one engraftment marker detected is at least one positive angiogenic marker and at least one positive extracellular matrix marker.
 13. The method of claim 6, wherein the at least one positive angiogenic marker is selected from the group consisting of: FGF10, PRKD1, CCBE1, PDGFRA, EPHB2, GATA2, NTRK1, PTGIS, BMPER, BMP4, C1GALT1, MEIS1, TBX1, PKNOX1, ID1, TCF21, HEY1, HOXB3, HGF, IL6, GHRL, IHH, SRPK2, GATA6, HAND1, AMOT, NRP2, PTEN, SEMA3E, APOLD1, SETD2, DAB2IP, KDR, PGF, EMP2, TAL1, ACVR1, HIPK2, CSPG4, TNFAIP3, NRP1, NFATC4, CDC42, ANGPTL4, BCAS3, HIPK1, NRXN3, FZD5 and HHEX. 14.-15. (canceled)
 16. The method of claim 9, wherein the at least one positive extracellular matrix marker is selected from the group consisting of: FGF10, SMOC1, CCBE1, COL6A6, ADAMTS12, COL19A1, LAMA1, BMP4, FBLN7, FBLN2, NDNF, HTRA1, HAPLN1, EMILIN1, SPOCK3, PODNL1, IHH, ACAN, NID2, COL4A6, LAMC1, FMOD, MUC4, EMID1, HMCN1, NID1, VCAN, CILP2, SOD3, ADAMTS3, ZP3, ANGPTL4, CRTAC1, LTBP4 and FREM1. 17.-18. (canceled)
 19. The method of claim 12, wherein: the at least one positive angiogenic marker is selected from the group consisting of: FGF10, PRKD1, CCBE1, PDGFRA, EPHB2, GATA2, NTRK1, PTGIS, BMPER, BMP4, C1GALT1, MEIS1, TBX1, PKNOX1, ID1, TCF21, HEY1, HOXB3, HGF, IL6, GHRL, IHH, SRPK2, GATA6, HAND1, AMOT, NRP2, PTEN, SEMA3E, APOLD1, SETD2, DAB2IP, KDR, PGF, EMP2, TAL1, ACVR1, HIPK2, CSPG4, TNFAIP3, NRP1, NFATC4, CDC42, ANGPTL4, BCAS3, HIPK1, NRXN3, FZD5 and HHEX; and the at least one positive extracellular matrix marker is selected from the group consisting of: FGF10, SMOC1, CCBE1, COL6A6, ADAMTS12, COL19A1, LAMA1, BMP4, FBLN7, FBLN2, NDNF, HTRA1, HAPLN1, EMILIN1, SPOCK3, PODNL1, IHH, ACAN, NID2, COL4A6, LAMC1, FMOD, MUC4, EMID1, HMCN1, NID1, VCAN, CILP2, SOD3, ADAMTS3, ZP3, ANGPTL4, CRTAC1, LTBP4 and FREM1. 20.-21. (canceled)
 22. The method of claim 31, wherein the at least one engraftment marker detected is at least one negative angiogenic marker.
 23. The method of claim 31, wherein the at least one engraftment marker detected is at least one negative extracellular matrix marker.
 24. The method of claim 31, wherein the at least one engraftment marker detected is at least one negative angiogenic marker and at least one negative extracellular matrix marker.
 25. The method of claim 22, wherein the at least one negative angiogenic marker is selected from the group consisting of: ETS1, BAX, XBP1, TDGF1, C5AR1, EPHA1, HS6ST1, SHC1, SP100, JAM3, CASP8, FLT4, SFRP2, HPSE, BAK1, GPX1, VAV3, VAV2, EGF, ADAM15 and AGGF1.
 26. (canceled)
 27. The method of claim 23, wherein the at least one negative extracellular matrix marker is selected from the group consisting of: FKBP1A, CLU, TFP12, PLSCR1, FBLN5, VWA1, ADAMTS16, MMP25, SFRP2 and SOD1.
 28. The method of claim 24, wherein: the at least one negative angiogenic marker is selected from the group consisting of: ETS1, BAX, XBP1, TDGF1, C5AR1, EPHA1, HS6ST1, SHC1, SP100, JAM3, CASP8, FLT4, SFRP2, HPSE, BAK1, GPX1, VAV3, VAV2, EGF, ADAM15 and AGGF1; and the at least one negative extracellular matrix marker is selected from the group consisting of: FKBP1A, CLU, TFP12, PLSCR1, FBLN5, VWA1, ADAMTS16, MMP25, SFRP2 and SOD1.
 29. The method of claim 31, wherein detecting expression of at least one engraftment marker comprises detecting expression of mRNA encoding the at least one engraftment marker in the HVPs.
 30. The method of claim 31, wherein detecting expression of at least one engraftment marker comprises detecting lack of expression of mRNA encoding the at least one engraftment marker in the HVPs.
 31. A method of identifying engraftable human ventricular progenitor cells (HVPs), the method comprising: subjecting human pluripotent stem cells to activation of Wnt/β-catenin signaling on day 0 of culture, followed by inhibition of Wnt/β-catenin signaling from day 3 to day 5 of culture to thereby obtain a culture of cardiac progenitor cells (CPCs) comprising LIFR+ Islet 1+ human ventricular progenitor cells (HVPs); isolating the LIFR+ Islet1+ HVPs on day 5, day 6 or day 7 of culture; and detecting expression of at least one engraftment marker on the LIFR+ Islet1+ HVPs to thereby detect the engraftable HVPs. 